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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980529Generated: October 26, 2026

Trichloro(chloromethyl)silane → Silane, dichloro(chloromethyl)phenyl-

https://huagongshe.com/reaction/1980529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloro(chloromethyl)silaneHCID 15258—
ReactantHCID 178506676HCID 178506676—
SolventTetrahydrofuranHCID 8028—
ProductSilane, dichloro(chloromethyl)phenyl-HCID 1274700729%

Reaction Steps

A solution of 25.1 ml (36.8 g, 0.200 mol) of chloromethyltrichlorosilane in 400 ml dry tetrahydrofuran was cooled to -78° under nitrogen and stirred vigorously while 48.0 ml (0.100 mol) of 2.1 molar phenyllithium was slowly dripped in over 1 hour. After stirring another 30 minutes at -78° the solution was allowed to warm to room temperature and evaporated to about 200 ml. Addition of 500 ml ether, filtration to remove precipitated lithium chloride, and evaporation of the filtrate left 25.0 g of liquid. Distillation gave 6.5 g (29%) of the title compound as a colorless liquid: bp 62°-82° (0.15 mm); nmr (CDCl3): δ3.3 (s, 2) and 7.1-7.9 (m, 5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04510136
Source datasetuspto-grants-1985_04
ORD IDord-c3753a67601a481f8f676519bccbe353
Source noteuspto-grants-1985_04