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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006069Generated: October 30, 2026

Triethylamine → 3-(2-Chloroethyl)-N-[3-(tert-butyldimethylsiloxy-methyl)benzyl]benzamide

https://huagongshe.com/reaction/1006069

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-(tert-Butyldimethylsiloxymethyl)benzylamineHCID 22049979—
Reactant3-(2-Chloroethyl)benzoyl chlorideHCID 22675358—
SolventEthyl AcetateHCID 8857—
Product3-(2-Chloroethyl)-N-[3-(tert-butyldimethylsiloxy-methyl)benzyl]benzamideHCID 2267536875%

Reaction Steps

A solution of 3-(2-chloroethyl)benzoyl chloride (2.43 g, 12.0 mmol) in ethyl acetate (10 mL) was added to a solution of 3-(tert-butyldimethylsiloxymethyl)benzylamine (3.01 g, 12.0 mmol) and triethylamine (3.3 mL, 24 mmol) in ethyl acetate (20 mL) at 0° C., and the resulting mixture was stirred at the same temperature for 2 hours and then at room temperature for 3 hours. The reaction mixture was diluted with ethyl acetate, washed successively with a 5% aqueous potassium hydrogensulfate solution, water, a saturated aqueous sodium hydrogencarbonate solution and a saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The residue was purified by a silica gel column chromatography (silica gel 200 mL; hexane/ethyl acetate=10/1 to 3/1) to obtain the title compound (3.74 g, 75%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787560B2
Source datasetuspto-grants-2004_09
ORD IDord-569b4340983b4f61bd43fecc721372ac
Source noteuspto-grants-2004_09