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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2058293Generated: October 30, 2026

Chlorotrimethylsilane → 4-(2-Methylpropyl)-beta,beta-bis(trimethylsiloxy)styrene

https://huagongshe.com/reaction/2058293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantDiisopropylamineHCID 7912—
ReactantHexaneHCID 8058—
ReactantIbufenacHCID 15250—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4-(2-Methylpropyl)-beta,beta-bis(trimethylsiloxy)styreneHCID 1260209970.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

Butyllithium in hexane (175 ml of 1.6 M solution, 0.28 mol) was added to a solution of 30 g (0.3 mol) of diisopropylamine in 200 ml of tetrahydrofuran at 25° C. The reaction mixture was cooled to 0° C. and a solution of 26.0 g (0.135 mol) of 4-(2-methylpropyl)benzeneacetic acid in 200 ml of tetrahydrofuran was added dropwise near 0° C. The mixture was stirred for 1 hour at 0° C. and then 70 ml (0.55 mol) of trimethylchlorosilane were added. The reaction mixture was warmed to room temperature and stirred for 2 hours. The solid that formed was filtered off; the filtrate was concentrated under reduced pressure and then mixed with 100 ml of diethyl ether. The resultant mixture was filtered and the filtrate was concentrated. Distillation of the residue gave 31.92 g (70% yield) of 4-(2-methylpropyl)-β,β-bis(trimethylsiloxy)styrene as a colorless liquid: bp 128° -130° C. (0.4 mm); ir (liquid) 6.07μ (C=C). Anal. Calcd. for C18H32O2Si2 : C, 64.22; H, 9.58; Found: C, 64.34; H, 9.95.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04215044
Source datasetuspto-grants-1980_07
ORD IDord-69cfc69d56b04669868c4963961092e6
Source noteuspto-grants-1980_07