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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2257417Generated: November 2, 2026

Benzylamine → N-[(Trimethylsilyl)methyl]benzylamine

https://huagongshe.com/reaction/2257417

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 numberUSRE035593
Source datasetuspto-grants-1997_08
ORD IDord-228af4b9686e4c2fb2d923f0471d1cd5
Source noteuspto-grants-1997_08