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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228871Generated: October 30, 2026

Triethylamine → Benzamide

https://huagongshe.com/reaction/2228871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Reactant2-Methylbenzoyl chlorideHCID 70276—
SolventDichloromethaneHCID 6344—
ProductBenzamideHCID 2331337.5%

Reaction Steps

To a solution of 391 mg (1 mmol) of 2R-hydroxy-3-[(2-methylpropyl)(4-aminophenyl)sulfonyl]amino-1S-(phenylmethyl)propylamine in 3 mL of anhydrous methylene chloride, was added 0.42 mL (3 mmol) of triethylamine, then at room temperature, 0.12 mL (0.9 mmol) of ortho-toluoyl chloride was added. After 15 hours at room temp ethyl acetate was added, washed with 5% citric acid, saturated sodium bicarbonate, brine, dried, filtered and concentrated to afford 420 mg of crude material. This was chromatographed on 40 g of silica gel using 50% ethyl acetate/hexane to afford 368 mg of pure benzamide, N-[2R-hydroxy-3-[[(4-aminophenyl)sulfonyl](2-methylpropyl)amino]-1S-(phenylmethyl)propyl]-2-methyl, m/e=516(M+Li).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06417387B1
Source datasetuspto-grants-2002_07
ORD IDord-f2ce2fd430d34be4939cc4d57e7a0481
Source noteuspto-grants-2002_07