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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382227Generated: October 25, 2026

N-Allyl-1,1,1-trimethyl-N-(trimethylsilyl)silylamine → N-trimethylsilyl-2-chloro-2-methy-1-aza-2-silacyclopentane

https://huagongshe.com/reaction/2382227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Allyl-1,1,1-trimethyl-N-(trimethylsilyl)silylamineHCID 82125—
Reactant(Dichloromethyl)silaneHCID 57353436—
SolventO-XyleneHCID 7237—
ProductN-trimethylsilyl-2-chloro-2-methy-1-aza-2-silacyclopentaneHCID 67301002—

Reaction Conditions

Temperature65 °C

Reaction Steps

N-trimethylsilyl-2-chloro-2-methy-1-aza-2-silacyclopentane (cyclic APMCS, which may be referred to as c-APMCS) was prepared as follows. To a 300 mL nitrogen purged bottle equipped with stir bar was added 20.1 g (0.1 mol) of N,N-bis(trimethylsilyl)allyl amine, 11.5 g (0.1 mol) of dichloromethylsilane, and 0.81 mL of 2.4 wt % Karsted's Catalyst in xylene. The solution was stirred for 72 hrs, then heated at 65° C. for 2 hrs, and heated at 100° C. for a further 3 days. The product was distilled at 85-90° C. at 25 mm Hg. GC/MS confirmed structure. Proton NMR was also used to determine structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258332B2
Source datasetuspto-grants-2012_09
ORD IDord-7b068095cd93427aadd57b2c0f15b16d
Source noteuspto-grants-2012_09