Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971618Generated: October 30, 2026

Methyldichlorosilane → HCID 86736577, compound

https://huagongshe.com/reaction/971618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyldichlorosilaneHCID 6376—
ReactantAllyl chlorideHCID 7850—
Reactant3-Chloro-2-methyl-1-propeneHCID 11241—
ReactantTrichlorosilaneHCID 24811—
ReactantChlorodimethylsilaneHCID 66108—
ReactantDiethyl(methyl)silaneHCID 69799—
ReactantDeuterotrichlorosilaneHCID 12432766—
ProductHCID 86736577HCID 8673657745%

Reaction Steps

Reactions of methallyl chloride with methyldichlorosilane and ethyldichlorosilane are reported in Chem. Abstract 50, 13726e (1956). The reaction of methyldichlorosilane with allyl chloride using chloroplatinic acid catalyst is reported to give a 40 percent yield of chloropropylmethyldichlorosilane, while the corresponding methallyl chloride reaction yields 70 percent of chloroisobutylmethyldichlorosilane (see Chem. Abstract 54, 22328b (1960). Higher yields of expected products were reported for methallyl chloride over allyl chloride in reactions with trichlorosilane, methyldichlorosilane, and dimethylchlorosilane in J. Am. Chem. Soc., 82, 3601 (1960), and indicated for the same reaction with deuterotrichlorosilane (Cl3SiD) in J. Am. Chem. Soc., 86, 895 (1964) (see also U.S. Pat. No. 3,686,253). The reaction of methallyl chloride with diethylmethylsilane gives 45 percent of chloroisobutyldiethylmethylsilane according to Chem. Abstracts 55, 15331c (1961). The preparation of siloxanes (as opposed to silanes) containing chloroisobutyl groups is disclosed in J. Am. Chem. Soc., 82, 3601 (1960).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04160775
Source datasetuspto-grants-1979_07
ORD IDord-08b1a6b78fb74ef699638c70f4f3e37e
Source noteuspto-grants-1979_07