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

2,2'-Bis(benzylphenylphosphinomethyl)-1,1'-biphenyl

中文名称
——
中文别名
——
英文名称
2,2'-Bis(benzylphenylphosphinomethyl)-1,1'-biphenyl
英文别名
Benzyl-[[2-[2-[[benzyl(phenyl)phosphanyl]methyl]phenyl]phenyl]methyl]-phenylphosphane
2,2'-Bis(benzylphenylphosphinomethyl)-1,1'-biphenyl化学式
CAS
——
化学式
C40H36P2
mdl
——
分子量
578.673
InChiKey
CCFYOLQKXGIGPI-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):
    8.7
  • 重原子数:
    42
  • 可旋转键数:
    11
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

点击查看最新优质反应信息

文献信息

  • Low pressure hydroformylation of dienes
    申请人:Eastman Kodak Company
    公开号:US04742178A1
    公开(公告)日:1988-05-03
    A hydroformylation process for preparing dialdehydes from dienes by contacting a C.sub.6 -C.sub.10 diene in a reaction zone at a temperature of from about 20.degree. C. to about 250.degree. C. and a pressure of from about 15 psig to about 800 psig with hydrogen, carbon monoxide, and a catalyst containing rhodium, the ligand having the formula ##STR1## wherein: n is 1-4; each R is independently selected from hydrogen, alkyl, alkoxy, aryloxy, aryl, aralkyl, alkaryl, alkoxyalkyl, cycloaliphatic, halogen, alkanoyl, alkanoyloxy, alkoxycarbonyl, carboxyl or cyano; each R.sub.1 and R.sub.2 is independently selected from alkyl, aryl, aralkyl, alkaryl or cycloaliphatic; each R.sub.3 and R.sub.4 is independently selected from hydrogen and the R.sub.1 substituents; and each Y is independently selected from the elements N, P, As, Sb and Bi.
    一种从双烯通过将C.sub.6 -C.sub.10双烯与氢气、一氧化碳和含有铑的催化剂在反应区域中接触,以在约20°C至约250°C的温度和约15 psig至约800 psig的压力下制备二醛的氢甲酰化过程,其中该配体具有以下式:其中:n为1-4;每个R独立地选择自氢、烷基、烷氧基、芳氧基、芳基、芳基烷基、烷基芳基、烷氧基烷基、环脂肪、卤素、烷酰、烷酰氧基、烷氧基羰基、羧基或氰基;每个R.sub.1和R.sub.2独立地选择自烷基、芳基、芳基烷基、烷基芳基或环脂肪;每个R.sub.3和R.sub.4独立地选择自氢和R.sub.1取代基;每个Y独立地选择自N、P、As、Sb和Bi元素。
  • Chelate ligands for low pressure hydroformylation catalyst and process
    申请人:Eastman Kodak Company
    公开号:US04694109A1
    公开(公告)日:1987-09-15
    A novel ligand for use in hydroformylation reactions wherein at least one olefin having from 2 to 20 carbon atoms is contacted in a reaction zone at a temperature of from about 20.degree. C. to about 250.degree. C. and a pressure of from about 50 psig to about 800 psig with hydrogen, carbon monoxide, and a catalyst containing rhodium, the ligand having the formula ##STR1## wherein: n is 1-4; each R is independently selected from hydrogen, alkyl, alkoxy, aryloxy, aryl, aralkyl, alkaryl, alkoxyalkyl, cycloaliphatic, halogen, alkanoyl, alkanoyloxy, alkoxycarbonyl, carboxyl or cyano; each R.sub.1 and R.sub.2 is independently selected from alkyl, aryl, aralkyl, alkaryl or cycloaliphatic; each R.sub.3 and R.sub.4 is independently selected from hydrogen and the R.sub.1 substituents; and each Y is independently selected from the elements N, P, As, Sb and Bi.
    一种新型配体,用于在反应区中将至少含有2至20个碳原子的烯烃与氢气、一氧化碳和含有铑的催化剂接触,反应温度在约20℃至约250℃之间,压力在约50 psig至约800 psig之间,该配体具有以下结构式:##STR1## 其中:n为1-4;每个R独立地选自氢、烷基、烷氧基、芳氧基、芳基、芳基烷基、烷基芳基、烷氧基烷基、环烷基、卤素、烷酰基、烷酰氧基、烷氧羰基、羧基或氰基;每个R.sub.1和R.sub.2独立地选自烷基、芳基、芳基烷基、烷基芳基或环烷基;每个R.sub.3和R.sub.4独立地选自氢和R.sub.1取代基;每个Y独立地选自元素N、P、As、Sb和Bi。
  • Preparation of bidentate ligands
    申请人:EASTMAN KODAK COMPANY
    公开号:EP0375576A1
    公开(公告)日:1990-06-27
    A process is disclosed for preparing bidentate ligands of the formula: wherein: each of Ar, R′, R˝ and Y are specifically defined species; the x bonds and the y bonds are attached to adjacent carbon atoms on the ring structures; and n is a whole number in the range of 0-4 where Ar is phenyl: 0-6 where Ar is naphthyl: and 0-8 where Ar is phenanthryl or anthracenyl. The invention process comprises a. reductively coupling an ortho-substituted aromatic moiety to produce a biphenyl compound; b. contacting the biphenyl compound produced in Step (a) with an anion having the structure: wherein Y, Y′ and R′ are specifically defined species; under conditions appropriate to form said bidentate ligand or the dioxide precursor thereof; and c. optionally reducing the intermediate product when the oxy-anion, is employed as the anion in Step (b).
    本发明公开了一种制备双取代配体的方法,其化学式为:其中:Ar、R'、R˝和Y分别是特定定义的物种;x键和y键连接在环结构上相邻的碳原子上;n是整数,在Ar为苯基时为0-4,在Ar为萘基时为0-6,在Ar为菲基或蒽基时为0-8。该发明方法包括:a. 还原偶氮苯衍生物,以产生联苯化合物;b. 将步骤(a)中产生的联苯化合物与具有以下结构的负离子接触:其中Y、Y'和R'是特定定义的物种;在适当的条件下形成所述双取代配体或其二氧化物前体;c. 当氧负离子在步骤(b)中作为负离子时,可选择性地还原中间产物。
  • Preparation of biaryl compounds
    申请人:EASTMAN KODAK COMPANY
    公开号:EP0376856A1
    公开(公告)日:1990-07-04
    A method for the preparation of biaryl compounds is disclosed which comprises contacting an aromatic halide in the presence of a catalyst comprising zerovalent nickel, a bidentate phosphorus-containing coordinating ligand and a reducing metal in a polar, aprotic solvent system for a time and under conditions suitable for the formation of biaryl compound.
    本发明公开了一种制备双芳基化合物的方法,该方法包括在极性烷基溶剂体系中,在适合形成双芳基化合物的时间和条件下,在由零价镍、双叉含磷配位体和还原金属组成的催化剂存在下,使芳香卤化物与催化剂接触。
  • DEVON, THOMAS J.;PHILLIPS, GERALD W.;PUCKETTE, THOMAS A.;STAVINOHA, JEROM+
    作者:DEVON, THOMAS J.、PHILLIPS, GERALD W.、PUCKETTE, THOMAS A.、STAVINOHA, JEROM+
    DOI:——
    日期:——
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)-(-)-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)-(+)-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)-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 (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 (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 (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-[[[[[[((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 (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 (-)-去甲基西布曲明 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫 龙胆紫 齐达帕胺 齐诺康唑 齐洛呋胺 齐墩果-12-烯[2,3-c][1,2,5]恶二唑-28-酸苯甲酯 齐培丙醇 齐咪苯 齐仑太尔 黑染料 黄酮,5-氨基-6-羟基-(5CI) 黄酮,6-氨基-3-羟基-(6CI) 黄蜡,合成物 黄草灵钾盐