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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982129Generated: October 28, 2026

Benzylamine → N-[(Trimethylsilyl)methyl]benzylamine

https://huagongshe.com/reaction/982129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantSilane, (chloromethyl)trimethyl-HCID 75361—
SolventSodium HydroxideHCID 14798—
ProductN-[(Trimethylsilyl)methyl]benzylamineHCID 353458—

Reaction Conditions

Temperature10 °C

Reaction Steps

A mixture of 264 mL (2.42 mol) of benzylamine and 97.7 g. (0.796 mol) of chloromethyltrimethylsilane was heated to 200° C. for 2.5 h and then cooled to 10° C. A 0.1M sodium hydroxide solution (400 mL) was added and the product was extracted with 3×200 mL of diethyl ether. The combined organic phase was washed with 100 mL of water, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The product was distilled at 115°-125° C. and 5 mm of Hg to afford the title compound as a clear liquid. 1H NMR (CDCl3) δ0.0 (s, 9H), 1.1 (br s, 1H), 2.01 (s, 2H), 3.76 (s, 2H), 7.1-7.3 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04994486
Source datasetuspto-grants-1991_02
ORD IDord-89363de4ef9c45599aac39de098c2e06
Source noteuspto-grants-1991_02