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外消旋-反式-1,2-双[二(3,5-二甲基苯基)膦基甲基]环丁烷 | 1226906-44-0

中文名称
外消旋-反式-1,2-双[二(3,5-二甲基苯基)膦基甲基]环丁烷
中文别名
——
英文名称
racemic-trans-1,2-Bis[di(3,5-dimethylphenyl)phosphinomethyl]cyclobutane
英文别名
[2-[bis(3,5-dimethylphenyl)phosphanylmethyl]cyclobutyl]methyl-bis(3,5-dimethylphenyl)phosphane
外消旋-反式-1,2-双[二(3,5-二甲基苯基)膦基甲基]环丁烷化学式
CAS
1226906-44-0
化学式
C38H46P2
mdl
——
分子量
564.7
InChiKey
REZOVLQIMMUCQH-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):
    9.8
  • 重原子数:
    40
  • 可旋转键数:
    8
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.37
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

文献信息

  • PRODUCING BDO VIA HYDROFORMYLATION OF ALLYL ALCOHOL MADE FROM GLYCERIN
    申请人:Lyondell Chemical Technology, L.P.
    公开号:US20190263737A1
    公开(公告)日:2019-08-29
    A method including hydroformylating, with syngas, allyl alcohol in an allyl alcohol feed, to produce a hydroformylation product comprising 4-hydroxybutyraldehyde and 3-hydroxy-2-methylpropionaldehyde; and producing a 1,4-butanediol (BDO) product comprising BDO and 1,3-methylpropanediol via hydrogenation of at least a portion of the hydroformylation product. A method including hydroformylating, with syngas, allyl alcohol in a feed comprising bio-allyl alcohol, to produce a hydroformylation product comprising 4-hydroxybutyraldehyde and 3-hydroxy-2-methylpropionaldehyde; and producing a BDO product comprising BDO and 1,3-methylpropanediol via hydrogenation of at least a portion of the hydroformylation product. A method including hydroformylating, with syngas, bio-allyl alcohol in a feed comprising bio-allyl alcohol, to produce a hydroformylation product comprising 4-hydroxybutyraldehyde and 3-hydroxy-2-methylpropionaldehyde; producing a BDO product comprising BDO and 1,3-methylpropanediol via hydrogenation of at least a portion of the hydroformylation product; and removing a byproduct of the production of the bio-allyl alcohol prior to hydroformylating the bio-allyl alcohol and/or from the BDO-product.
    一种方法包括使用合成气对丙烯醇进行氢甲酰化,以产生含有4-羟基丁醛和3-羟基-2-甲基丙醛的氢甲酰化产物;并通过对至少部分氢甲酰化产物进行加氢,生产包括丁二醇和1,3-甲基丙二醇1,4-丁二醇BDO)产品。一种方法包括使用合成气对含有生物丙烯醇的进料中的丙烯醇进行氢甲酰化,以产生含有4-羟基丁醛和3-羟基-2-甲基丙醛的氢甲酰化产物;并通过对至少部分氢甲酰化产物进行加氢,生产包括丁二醇和1,3-甲基丙二醇BDO产品。一种方法包括使用合成气对含有生物丙烯醇的进料中的生物丙烯醇进行氢甲酰化,以产生含有4-羟基丁醛和3-羟基-2-甲基丙醛的氢甲酰化产物;通过对至少部分氢甲酰化产物进行加氢,生产包括丁二醇和1,3-甲基丙二醇BDO产品;并在氢甲酰化生产生物丙烯醇之前或从BDO产品中去除生物丙烯醇生产的副产物。
  • High linear selectivity ligand for allyl alcohol hydroformylation
    申请人:Lyondell Chemical Technology, L.P.
    公开号:US10807934B1
    公开(公告)日:2020-10-20
    A process for selectively producing 4-hydroxybutyraldehyde from allyl alcohol is described. The process comprises reacting allyl alcohol with a mixture of carbon monoxide and hydrogen in the presence of a solvent and a catalyst system comprising a rhodium complex and a trans-1,2-bis(bis(3,4,5-tri-n-alkylphenyl)phosphinomethyl)-cyclobutane. The process gives high yield of 4-hydroxybutyraldehyde compared to temperature.
    本发明描述了一种从丙烯醇选择性地生产4-羟基丁醛的过程。该过程包括在溶剂和催化剂体系的存在下,将丙烯醇与一种混合物(包括一氧化碳氢气)反应,所述催化剂体系包括一个配合物和一个trans-1,2-双(双(3,4,5-三-n-烷基苯基)酰甲基)环丁烷。与温度相比,该过程可以高产得4-羟基丁醛
  • IMPROVING RHENIUM CATALYSTS FOR GLYCERIN TO ALLYL ALCOHOL CONVERSION
    申请人:Lyondell Chemical Technology, L.P.
    公开号:EP3530644A1
    公开(公告)日:2019-08-28
    A catalyst system for the conversion of glycerin to allyl alcohol, the catalyst system comprising: a rhenium compound selected from rhenium dioxide, rhenium trioxide, and a combination thereof. A method of producing allyl alcohol from glycerin via the catalyst system, the method comprising exposing glycerin to a temperature of greater than 140°C in the presence of a catalyst comprising rhenium trioxide, rhenium dioxide, or a combination thereof to produce a product comprising allyl alcohol.
    一种将甘油转化为烯丙基醇的催化剂系统,该催化剂系统包括:选自二氧化铼、三氧化铼及其组合的化合物。一种通过催化剂系统从甘油中生产烯丙醇的方法,该方法包括在由三氧化铼、二氧化铼或它们的组合组成的催化剂存在下,将甘油暴露在高于140℃的温度下,以生产包含烯丙醇的产品。
  • Producing BDO via hydroformylation of allyl alcohol made from glycerin
    申请人:Lyondell Chemical Technology, L.P.
    公开号:US10919023B2
    公开(公告)日:2021-02-16
    A method including hydroformylating, with syngas, allyl alcohol in an allyl alcohol feed, to produce a hydroformylation product comprising 4-hydroxybutyraldehyde and 3-hydroxy-2-methylpropionaldehyde; and producing a 1,4-butanediol (BDO) product comprising BDO and 1,3-methylpropanediol via hydrogenation of at least a portion of the hydroformylation product. A method including hydroformylating, with syngas, allyl alcohol in a feed comprising bio-allyl alcohol, to produce a hydroformylation product comprising 4-hydroxybutyraldehyde and 3-hydroxy-2-methylpropionaldehyde; and producing a BDO product comprising BDO and 1,3-methylpropanediol via hydrogenation of at least a portion of the hydroformylation product. A method including hydroformylating, with syngas, bio-allyl alcohol in a feed comprising bio-allyl alcohol, to produce a hydroformylation product comprising 4-hydroxybutyraldehyde and 3-hydroxy-2-methylpropionaldehyde; producing a BDO product comprising BDO and 1,3-methylpropanediol via hydrogenation of at least a portion of the hydroformylation product; and removing a byproduct of the production of the bio-allyl alcohol prior to hydroformylating the bio-allyl alcohol and/or from the BDO-product.
    一种方法,包括用合成气将烯丙基醇进料中的烯丙基醇进行加氢甲酰化,生成包括4-羟基丁醛和3-羟基-2-甲基丙醛的加氢甲酰化产物;以及通过对至少一部分加氢甲酰化产物进行氢化,生成包括BDO和1,3-甲基丙二醇1,4-丁二醇BDO)产物。一种方法,包括用合成气对包含生物烯丙基醇的进料中的烯丙基醇进行加氢甲酰化,生成包含 4-羟基丁醛和 3-羟基-2-甲基丙醛的加氢甲酰化产物;以及通过加氢甲酰化产物的至少一部分进行氢化,生成包含 BDO 和 1,3-甲基丙二醇BDO 产物。一种方法,包括在包含生物烯丙基醇的进料中用合成气对生物烯丙基醇进行加氢甲酰化,以生产包含 4-羟基丁醛和 3-羟基-2-甲基丙醛的加氢甲酰化产物;通过加氢甲酰化产物中至少一部分的氢化反应,生产由 BDO 和 1,3-甲基丙二醇组成的 BDO 产物;以及在对生物烯丙基醇进行加氢甲酰化之前和/或从 BDO 产物中去除生产生物烯丙基醇的副产物。
  • Rhenium catalysts for glycerin to allyl alcohol conversion
    申请人:Lyondell Chemical Technology, L.P.
    公开号:US10919024B2
    公开(公告)日:2021-02-16
    A catalyst system for the conversion of glycerin to allyl alcohol, the catalyst system comprising: a rhenium compound selected from rhenium dioxide, rhenium trioxide, and a combination thereof. A method of producing allyl alcohol from glycerin via the catalyst system, the method comprising exposing glycerin to a temperature of greater than 140° C. in the presence of a catalyst comprising rhenium trioxide, rhenium dioxide, or a combination thereof to produce a product comprising allyl alcohol.
    一种将甘油转化为烯丙基醇的催化剂系统,该催化剂系统包括:选自二氧化铼、三氧化铼及其组合的化合物。一种通过催化剂系统从甘油生产烯丙醇的方法,该方法包括在由三氧化铼、二氧化铼或它们的组合组成的催化剂存在下,将甘油暴露在高于140℃的温度下,以生产包含烯丙醇的产品。
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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