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

1-Butene,4,4-diacetyloxy-

中文名称
——
中文别名
——
英文名称
1-Butene,4,4-diacetyloxy-
英文别名
1-acetyloxybut-3-enyl acetate
1-Butene,4,4-diacetyloxy-化学式
CAS
——
化学式
C8H12O4
mdl
——
分子量
172.181
InChiKey
YXZWFBWVGCBLHO-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):
    1.3
  • 重原子数:
    12
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    52.6
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

点击查看最新优质反应信息

文献信息

  • Palladium-catalyzed intramolecular olefin allylations: Stereocontrolled syntheses of bicyclic systems and evidence for an allylpalladium/olefin-cis-insertion
    作者:Wolfgang Oppolzer、Jean-Marc Gaudin、Timothy N. Birkinshaw
    DOI:10.1016/s0040-4039(00)80586-9
    日期:——
    Pd(O)-catalyzed cyclizations of (1-acetoxy-3-alkenyl)-2-cycloalkenes , and provide bicyclic systems in high diastereo- (, ) and enantio-meric () purity consistent with a predominant allylpalladium/alkene cis- insertion.
    的Pd(O)催化的的环化(1-乙酰氧基-3-烯基)-2-环烯烃,和提供在高diastereo-双环系统(,)和对映聚体()纯度具有占优势的烯丙基/烯烃一致顺-插入。
  • PROCESSES FOR THE PREPARATION OF ORGANIC DIESTERS
    申请人:DAICEL CHEMICAL INDUSTRIES, Ltd.
    公开号:EP1044955A1
    公开(公告)日:2000-10-18
    The present invention relates a method of preparing an organic diester which comprises a first step (1) whom a diolefin and a peracid compound are allowed to react to synthesize a monoepoxide, a second step (2) wherein said synthesized monoepoxide is allowed to react with water and carboxylic acid and a third step (3) where the synthesized compounds are allowed to react with an acid anhydride. The present invention also relates to a method of preparing an organic diester wherein in the second step (2), the molar ratio of water and carboxylic acid added into monoepoxide is more than 2 and not more than 20, to an organic diester preparing method wherein monoepoxide is allowed to react with water in the second step (2) and to a method of preparing an organic diester wherein in the second step (2), water and carboxylic acid are removed from the synthesized product and recycled to be used again in said second step (2). The purpose of the present invention is to provide a method of preparing an organic diester having a good selectivity a producing few impurities and using diolefin as a starting material. In the second step (2), when water and carboxylic acid are recycled and used again, it is possible to reduce the load of dumping water and particularly, when 1, 3-butadiene is used as diolefin, acetic acid is used as carboxylic acid and acetic anhydride is used as an acid anhydride it is also possible to reduce the use amount of acetic acid.
    本发明涉及制备有机二酯的方法,包括第一步(1),在该步骤中,将二烯和过氧化物化合物反应以合成单环氧化物;第二步(2),在该步骤中,将合成的单环氧化物羧酸反应;第三步(3),将合成的化合物与酸酐反应。本发明还涉及一种制备有机二酯的方法,其中在第二步(2)中,加入到单环氧化物中的羧酸的摩尔比大于2且不大于20;一种有机二酯制备方法,其中单环氧化物在第二步(2)中与反应;以及一种制备有机二酯的方法,其中在第二步(2)中,从合成的产物中去除羧酸并回收以再次使用。本发明的目的是提供一种制备有机二酯的方法,该方法具有良好的选择性,产生少量杂质,并使用二烯作为起始材料。在第二步(2)中,当羧酸被回收并再次使用时,可以减少倾倒的负担,特别是当1,3-丁二烯被用作二烯,乙酸被用作羧酸乙酸酐被用作酸酐时,也可以减少乙酸的使用量。
  • Process for the oxyacylation of butenes to linear acetates
    申请人:Sun Refining and Marketing Company
    公开号:EP0144252A1
    公开(公告)日:1985-06-12
    C4 olefins comprising cis- and trans-butene-2 and butene-1 may be oxidized to their corresponding mono- and diacetates in the presence of acetic acid and an olefin-' activated palladium catalyst under mild conditions. With this catalyst, and depending in part upon the solvent employed, as well as other operating conditions, the formation of linear allylic 1-acetates over the corresponding branched compounds can be favoured in order to increase the yield of the corresponding linear 1,4-diacetates. The latter, in turn, may then be converted, for example, to butanediol by known hydrogenation methods. In a similar manner, isobutylene may be converted to a dialcohol.
    由顺式和反式丁烯-2 和丁烯-1 组成的 C4 烯烃可在乙酸和烯烃活化催化剂存在下,在温和条件下氧化成相应的单乙酸酯和二乙酸酯。 使用这种催化剂,并部分取决于所使用的溶剂以及其他操作条件,可以更有利于形成线性烯丙基 1-乙酸酯,而不是相应的支链化合物,以增加相应的线性 1,4-二乙酸酯的产量。 然后,后者可以通过已知的氢化方法转化为丁二醇等。 异丁烯也可以通过类似的方法转化为二元醇。
  • Process for preparing ethylene interpolymers and ethylene interpolymers obtained therefrom
    申请人:EASTMAN CHEMICAL COMPANY
    公开号:EP1195392A2
    公开(公告)日:2002-04-10
    There is desribed a novel process for preparing interpolymers comprising ethylene and at least two monomer units selected from heteroatom substituted olefin monomer units derived from a compound of the formula XV wherein E and G represent the same or different heteroatoms selected from oxygen, nitrogen, and sulfur, which are bound to a hydrogen atom, a hydrocarbyl group, or a substituted hydrocarbyl group, or are joined by a linking group; and n is 0 or an integer from 1-20; or 2,3-dihydrofuran, or vinylcyclopropane, and interpolymers prepared thereby, including novel interpolymers having melting peak temperatures (Tm) equal to or greater than 50°C.
    本发明描述了一种新型工艺,用于制备由乙烯和至少两个单体单元组成的互聚合物,这两个单体单元选自源自式 XV 化合物的杂原子取代的烯烃单体单元。 其中 E 和 G 代表选自氧、氮和的相同或不同的杂原子,它们与氢原子、烃基或取代的烃基结合,或由连接基团连接;n 为 0 或 1-20 之间的整数; 或 2,3-二氢呋喃,或乙烯基环丙烷,以及由此制备的互聚合物,包括熔融峰温度(Tm)等于或大于 50°C 的新型互聚合物。
  • A PROCESS FOR THE PREPARATION OF 1,4-DISUBSTITUTED 2-BUTENES
    申请人:EASTMAN KODAK COMPANY (a New Jersey corporation)
    公开号:EP0380578A1
    公开(公告)日:1990-08-08
查看更多

同类化合物

(甲基3-(二甲基氨基)-2-苯基-2H-azirene-2-羧酸乙酯) (±)-盐酸氯吡格雷 (±)-丙酰肉碱氯化物 (d(CH2)51,Tyr(Me)2,Arg8)-血管加压素 (S)-(+)-α-氨基-4-羧基-2-甲基苯乙酸 (S)-阿拉考特盐酸盐 (S)-赖诺普利-d5钠 (S)-2-氨基-5-氧代己酸,氢溴酸盐 (S)-2-[[[(1R,2R)-2-[[[3,5-双(叔丁基)-2-羟基苯基]亚甲基]氨基]环己基]硫脲基]-N-苄基-N,3,3-三甲基丁酰胺 (S)-2-[3-[(1R,2R)-2-(二丙基氨基)环己基]硫脲基]-N-异丙基-3,3-二甲基丁酰胺 (S)-1-(4-氨基氧基乙酰胺基苄基)乙二胺四乙酸 (S)-1-[N-[3-苯基-1-[(苯基甲氧基)羰基]丙基]-L-丙氨酰基]-L-脯氨酸 (R)-乙基N-甲酰基-N-(1-苯乙基)甘氨酸 (R)-丙酰肉碱-d3氯化物 (R)-4-N-Cbz-哌嗪-2-甲酸甲酯 (R)-3-氨基-2-苄基丙酸盐酸盐 (R)-1-(3-溴-2-甲基-1-氧丙基)-L-脯氨酸 (N-[(苄氧基)羰基]丙氨酰-N〜5〜-(diaminomethylidene)鸟氨酸) (6-氯-2-吲哚基甲基)乙酰氨基丙二酸二乙酯 (4R)-N-亚硝基噻唑烷-4-羧酸 (3R)-1-噻-4-氮杂螺[4.4]壬烷-3-羧酸 (3-硝基-1H-1,2,4-三唑-1-基)乙酸乙酯 (2S,4R)-Boc-4-环己基-吡咯烷-2-羧酸 (2S,3S,5S)-2-氨基-3-羟基-1,6-二苯己烷-5-N-氨基甲酰基-L-缬氨酸 (2S,3S)-3-((S)-1-((1-(4-氟苯基)-1H-1,2,3-三唑-4-基)-甲基氨基)-1-氧-3-(噻唑-4-基)丙-2-基氨基甲酰基)-环氧乙烷-2-羧酸 (2S)-2,6-二氨基-N-[4-(5-氟-1,3-苯并噻唑-2-基)-2-甲基苯基]己酰胺二盐酸盐 (2S)-2-氨基-N,3,3-三甲基-N-(苯甲基)丁酰胺 (2S)-2-氨基-3-甲基-N-2-吡啶基丁酰胺 (2S)-2-氨基-3,3-二甲基-N-(苯基甲基)丁酰胺, (2S)-2-氨基-3,3-二甲基-N-2-吡啶基丁酰胺 (2S,4R)-1-((S)-2-氨基-3,3-二甲基丁酰基)-4-羟基-N-(4-(4-甲基噻唑-5-基)苄基)吡咯烷-2-甲酰胺盐酸盐 (2R,3'S)苯那普利叔丁基酯d5 (2R)-2-氨基-3,3-二甲基-N-(苯甲基)丁酰胺 (2-氯丙烯基)草酰氯 (1S,3S,5S)-2-Boc-2-氮杂双环[3.1.0]己烷-3-羧酸 (1R,5R,6R)-5-(1-乙基丙氧基)-7-氧杂双环[4.1.0]庚-3-烯-3-羧酸乙基酯 (1R,4R,5S,6R)-4-氨基-2-氧杂双环[3.1.0]己烷-4,6-二羧酸 齐特巴坦 齐德巴坦钠盐 齐墩果-12-烯-28-酸,2,3-二羟基-,苯基甲基酯,(2a,3a)- 齐墩果-12-烯-28-酸,2,3-二羟基-,羧基甲基酯,(2a,3b)-(9CI) 黄酮-8-乙酸二甲氨基乙基酯 黄荧菌素 黄体生成激素释放激素(1-6) 黄体生成激素释放激素 (1-5) 酰肼 黄体瑞林 麦醇溶蛋白 麦角硫因 麦芽聚糖六乙酸酯 麦根酸