摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

4-(pentafluorophenylmethyl)-2-propiolactone | 1044747-43-4

中文名称
——
中文别名
——
英文名称
4-(pentafluorophenylmethyl)-2-propiolactone
英文别名
4-[(2,3,4,5,6-Pentafluorophenyl)methyl]oxetan-2-one;4-[(2,3,4,5,6-pentafluorophenyl)methyl]oxetan-2-one
4-(pentafluorophenylmethyl)-2-propiolactone化学式
CAS
1044747-43-4
化学式
C10H5F5O2
mdl
——
分子量
252.141
InChiKey
PEGNXGKFOQPKIM-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    2.3
  • 重原子数:
    17
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    7

反应信息

  • 作为产物:
    描述:
    2-(pentafluorophenylmethyl)oxirane一氧化碳 在 [(salph)Cr(THF)2]+[Co(CO)4]- 作用下, 以 乙二醇二甲醚 为溶剂, 25.0 ℃ 、689.49 kPa 条件下, 反应 6.0h, 以82%的产率得到4-(pentafluorophenylmethyl)-2-propiolactone
    参考文献:
    名称:
    Fluorinated β-lactones and poly(β-hydroxyalkanoate)s: synthesis via epoxide carbonylation and ring-opening polymerization
    摘要:
    Efficient and mild reaction conditions were developed for the catalytic carbonylation of fluorinated epoxides to their corresponding beta-lactones. Six new lactones with fluorinated side chains were prepared in high isolated yields. These lactones were polymerized to form a series of new poly(beta-hydroxy-alkanoate)s with fluorinated side chains, and their properties were examined with respect to their hydrocarbon analogs. Finally, copolymerizations were performed with fluorinated lactones and beta-butyrolactone, which resulted in tapered copolymers rather than the expected random copolymers. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2008.03.108
点击查看最新优质反应信息

文献信息

  • Acrylonitrile Derivatives from Epoxide and Carbon Monoxide Reagents
    申请人:Novomer, Inc.
    公开号:US20190002400A1
    公开(公告)日:2019-01-03
    The present invention is directed to reactor systems and processes for producing acrylonitrile and acrylonitrile derivatives. In preferred embodiments of the present invention, the processes comprise the following steps: introducing an epoxide reagent and carbon monoxide reagent to at least one reaction vessel through at least one feed stream inlet; contacting the epoxide reagent and carbon monoxide reagent with a carbonylation catalyst to produce a beta-lactone intermediate; polymerizing the beta-lactone intermediate with an initiator in the presence of a metal cation to produce a polylactone product; heating the polylactone product under thermolysis conditions to produce an organic acid product; optionally esterifying the organic acid product to produce one or more ester products; and reacting the organic acid product and/or ester product with an ammonia reagent under ammoxidation conditions to produce an acrylonitrile product.
    本发明涉及反应器系统和生产丙烯腈丙烯腈生物的工艺。在本发明的优选实施例中,该工艺包括以下步骤:将环试剂和一氧化碳试剂通过至少一个进料流入口引入至至少一个反应釜中;将环试剂和一氧化碳试剂与羰基化催化剂接触以产生β-内中间体;在属阳离子存在下,将β-内中间体引发剂聚合以产生聚内产品;在热解条件下加热聚内产品以产生有机酸产品;可选择化有机酸产品以产生一个或多个产品;并将有机酸产品和/或产品与试剂在化条件下反应以产生丙烯腈产品。
  • PROCESSES FOR PRODUCING BETA-LACTONE AND BETA-LACTONE DERIVATIVES WITH HETEROGENOUS CATALYSTS
    申请人:Novomer, Inc.
    公开号:US20190047972A1
    公开(公告)日:2019-02-14
    The present invention is directed to processes from producing beta-lactone and beta-lactone derivatives using heterogenous catalysts. In preferred embodiments of the present invention, the processes comprise the steps: passing a feed stream comprising an epoxide reagent and a carbon monoxide reagent to a reaction zone; contacting the epoxide reagent and the carbon monoxide reagent with a heterogenous catalyst to produce a beta-lactone product in the reaction zone; and removing the beta-lactone product from the reaction zone. In preferred embodiments, the heterogenous catalyst comprises a solid support containing a cationic Lewis acid functional group and a metal carbonyl compound comprising at least one of anionic metal carbonyl compound or a neutral metal carbonyl compound. In certain preferred embodiments, the epoxide reagent and carbon monoxide reagent have a biobased content.
    本发明涉及使用异质催化剂生产β-内和β-内生物的过程。在本发明的首选实施例中,该过程包括以下步骤:将包含环试剂和一氧化碳试剂的进料流通入反应区;将环试剂和一氧化碳试剂与异质催化剂接触,在反应区内产生β-内产物;并从反应区中移除β-内产物。在首选实施例中,异质催化剂包括固体支撑体,其中包含阳离子路易斯酸功能团和属羰基化合物,其中至少包括一种阴离子属羰基化合物或中性属羰基化合物。在某些首选实施例中,环试剂和一氧化碳试剂具有生物基含量。
  • Systems and processes for thermolysis of polylactones to produce organic acids
    申请人:Novomer, Inc.
    公开号:US10457624B2
    公开(公告)日:2019-10-29
    Reactor systems and processes produce organic acids through thermolysis of polylactones. The reactor systems and processes introduce at least one epoxide reagent and carbon monoxide reagent to at least one reaction vessel through at least one feed stream inlet. The epoxide reagent and carbon monoxide reagent contact at least one carbonylation catalyst to produce at least one beta-lactone intermediate. The beta-lactone intermediate is polymerized with at least one initiator in the presence of a metal cation to produce at least one polylactone product. The polylactone product is heated under thermolysis conditions to produce at least one organic acid product. The processes control the presence of contaminates, impurities, catalytic materials, and/or reagents to provide for highly pure organic acid products.
    反应器系统和工艺通过热分解聚内生产有机酸。反应器系统和工艺通过至少一个进料流入口将至少一种环试剂和一氧化碳试剂引入至少一个反应容器。环氧化物试剂和一氧化碳试剂与至少一种羰基化催化剂接触,生成至少一种β-内中间体。在属阳离子存在下,β-内中间体与至少一种引发剂聚合,生成至少一种聚内产品。聚内产品在热分解条件下加热,生成至少一种有机酸产品。这些工艺可控制污染物、杂质、催化材料和/或试剂的存在,以提供高纯度的有机酸产品。
  • Processes for producing beta-lactone with heterogenous catalysts
    申请人:Novomer, Inc.
    公开号:US10590099B1
    公开(公告)日:2020-03-17
    The present invention is directed to processes from producing beta-lactone and beta-lactone derivatives using heterogenous catalysts. In preferred embodiments of the present invention, the processes comprise the steps: passing a feed stream comprising an epoxide reagent and a carbon monoxide reagent to a reaction zone; contacting the epoxide reagent and the carbon monoxide reagent with a heterogenous catalyst to produce a beta-lactone product in the reaction zone; and removing the beta-lactone product from the reaction zone. In preferred embodiments, the heterogenous catalyst comprises a solid support containing a cationic Lewis acid functional group and a metal carbonyl compound comprising at least one of anionic metal carbonyl compound or a neutral metal carbonyl compound. In certain preferred embodiments, the epoxide reagent and carbon monoxide reagent have a biobased content.
    本发明涉及使用异质催化剂生产β-内和β-内生物的工艺。在本发明的优选实施方案中,该工艺包括以下步骤:将包含环氧化物试剂和一氧化碳试剂的进料流通入反应区;使环氧化物试剂和一氧化碳试剂与异质催化剂接触,在反应区生成β-内产物;从反应区除去β-内产物。在优选的实施方案中,异质催化剂包括含有阳离子路易斯酸官能团和属羰基化合物的固体载体,属羰基化合物包括阴离子属羰基化合物或中性属羰基化合物中的至少一种。在某些优选的实施方案中,环氧化物试剂和一氧化碳试剂具有生物基含量。
  • Acrylonitrile derivatives from epoxide and carbon monoxide reagents
    申请人:Novomer, Inc.
    公开号:US10676426B2
    公开(公告)日:2020-06-09
    The present invention is directed to reactor systems and processes for producing acrylonitrile and acrylonitrile derivatives. In preferred embodiments of the present invention, the processes comprise the following steps: introducing an epoxide reagent and carbon monoxide reagent to at least one reaction vessel through at least one feed stream inlet; contacting the epoxide reagent and carbon monoxide reagent with a carbonylation catalyst to produce a beta-lactone intermediate; polymerizing the beta-lactone intermediate with an initiator in the presence of a metal cation to produce a polylactone product; heating the polylactone product under thermolysis conditions to produce an organic acid product; optionally esterifying the organic acid product to produce one or more ester products; and reacting the organic acid product and/or ester product with an ammonia reagent under ammoxidation conditions to produce an acrylonitrile product.
    本发明涉及生产丙烯腈丙烯腈生物的反应器系统和工艺。在本发明的优选实施方案中,工艺包括以下步骤:通过至少一个进料流入口,将环试剂和一氧化碳试剂引入至少一个反应容器; 将环试剂和一氧化碳试剂与羰基化催化剂接触,生成β-内中间体; 在属阳离子存在下,将β-内中间体引发剂聚合,生成聚内产物;在热分解条件下加热聚内产品,生成有机酸产品;可选择将有机酸产品化,生成一种或多种产品;有机酸产品和/或产品在化条件下与试剂反应,生成丙烯腈产品。
查看更多

同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S,S)-邻甲苯基-DIPAMP (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(-)-4,12-双(二苯基膦基)[2.2]对环芳烷(1,5环辛二烯)铑(I)四氟硼酸盐 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(4-叔丁基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(3-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-4,7-双(3,5-二-叔丁基苯基)膦基-7“-[(吡啶-2-基甲基)氨基]-2,2”,3,3'-四氢1,1'-螺二茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (R)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4S,4''S)-2,2''-亚环戊基双[4,5-二氢-4-(苯甲基)恶唑] (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (3aR,6aS)-5-氧代六氢环戊基[c]吡咯-2(1H)-羧酸酯 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[((1S,2S)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1S,2S,3R,5R)-2-(苄氧基)甲基-6-氧杂双环[3.1.0]己-3-醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (1-(2,6-二氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙蒿油 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫-d6 龙胆紫