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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197824Generated: November 3, 2026

Benzylamine → N-[(Trimethylsilyl)methyl]benzylamine

https://huagongshe.com/reaction/1197824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantPotassium CarbonateHCID 11430—
ReactantSilane, (chloromethyl)trimethyl-HCID 75361—
ProductN-[(Trimethylsilyl)methyl]benzylamineHCID 353458—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of chloromethyltrimethylsilane (325 g, 370 ml, 2.65 mole) and benzylamine (835 g, 850 ml, 7.78 mole) was heated at 120° C. (oil bath temperature) for 2 h. A white solid began appearing after only 10 minutes and a viscous mixture eventually resulted. The reaction mixture was allowed to cool, then basified with potassium carbonate solution and extracted twice with ether. The combined extracts were dried (Na2SO4) and concentrated in vacuo to leave a yellow oil, which was purified by distillation. The excess benzylamine was removed in the first fractions (b.p. 47°-62° C. at 2 mmHg). The title compound (D11) was obtained as a colourless oil (380 g, 74%) b.p. 75°-80° C. at 2 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05278170
Source datasetuspto-grants-1994_01
ORD IDord-c4ca505839414dbaad96275cd21dc180
Source noteuspto-grants-1994_01