Styrene → 3,3-Dichloro-1,5-diphenyl-3-silahexane

HRID 1770330Notes

Reaction equation

HRID 1770330 reaction equation
[C:1]1([CH:7]([CH3:12])[CH2:8][SiH:9]([Cl:11])[Cl:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:13]=[CH:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>C(O)(C)C.[H+].[H+].Cl[Pt-2](Cl)(Cl)(Cl)(Cl)Cl>[Cl:10][Si:9]([Cl:11])([CH2:8][CH:7]([C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)[CH3:12])[CH2:13][CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1

Participants

5

Procedure

In the same apparatus and procedures as EXAMPLE 1, 10.0 g (0.046 mole) of 3-phenyl-1,1-dichloro-1-silabutane, 7.2 g (0.07 mole) of styrene, and 20 μl of 1% chloroplatinic acid in isopropanol were placed and reacted for 3 hours under the dry nitrogen atmosphere at 60° C. Vacuum distillation of the reaction products gave 11.0 g (bp, 133°-5° C./0.6 mmHg) of 3,3-dichloro-1,5-diphenyl-3-silahexane.

Workup

  1. customreacted for 3 hours under the dry nitrogen atmosphere at 60° C
  2. distillationVacuum distillation of the reaction products

Sources & evidence

ORD record
ord-5c2e2c3b54bd40c493888738b8b2837f
Source dataset
uspto-grants-1995_01
Patent number
US05386050

Reaction notes

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