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[1-(di-tert-butylphosphino)-3-ethoxyindene, P-Cr]pentacarbonylchromium | 159803-86-8

中文名称
——
中文别名
——
英文名称
[1-(di-tert-butylphosphino)-3-ethoxyindene, P-Cr]pentacarbonylchromium
英文别名
——
[1-(di-tert-butylphosphino)-3-ethoxyindene, P-Cr]pentacarbonylchromium化学式
CAS
159803-86-8
化学式
C24H29CrO6P
mdl
——
分子量
496.46
InChiKey
GDYSYSUSJOKTGX-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

反应信息

  • 作为产物:
    描述:
    (3-di-tert-butylphosphino-1-ethoxy-3-phenylpropenyllidene)pentacarbonylchromium 以 为溶剂, 生成 [1-(di-tert-butylphosphino)-3-ethoxyindene, P-Cr]pentacarbonylchromium
    参考文献:
    名称:
    通过过渡金属配合物进行有机合成。75.通过环烷基化碳烯络合物(M = Cr,W)进行环化反应生成的膦基萘和膦基茚
    摘要:
    1-Amino-2-ethoxy-4-phosphinonaphthalenes 6a,b (>90% yields) are obtained from (phenylalkynyl)carbene complexes (CO)(5)M=C(OEt)-C drop C-Ph (M = Cr, W) 1 by a novel two-step carbene/alkyne benzannulation, The first step involves the formation of(E)-(2-phenyl-2-phosphinoethenyl)carbene complexes (CO)5M=C(OEt)-CH=C(Ph)-PR(2) (E)-3a-c by 3-addition of secondary phosphines HPR(2) (R = t-Bu, c-C6W11) 2a,b to 1. A subsequent addition of isocyanides R(1)NC (R = t-Bu, c-C6H11) 4a,b to (E)-3a-c yields ketene imine complexes (Co)(5)M[R(1)N=C=C(OEt)-CH=C(Ph)-PR(2)] A by the ins ertion of 4 into the M=C bond of 3. (Metal-free) ketene imines are generated from A by ligand displacement with 4 and cyclize spontaneously to 6. Thermolysis of(E)3a-c affords (CO)(5)M phosphinoindene complexes 9 and 10. Reaction of 9 or 10 with pyridine yields phosphinoindenes 12 and pyridine complexes (CO)(5)M(C5H5N) 11. 10a, C24H29CrO6P, was characterized by X-ray diffraction. It crystallizes in space group P ($) over bar 1 No. 2 with cell parameters a = 9.412(1) Angstrom, b = 11.455(2) Angstrom, c 11.962(2) Angstrom, = 89.10(1)degrees, beta = 79.09(1)degrees, gamma = 88.60(1)degrees, Z = 2, R(1) = 0.063, and wR(2) = 0.117.
    DOI:
    10.1021/om00001a035
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