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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739766Generated: October 31, 2026

Triethylamine → Benzamide

https://huagongshe.com/reaction/1739766

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 orthotoluoyl 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 numberUS05968942
Source datasetuspto-grants-1999_10
ORD IDord-8af6144ba57f4bec8d505ea366254632
Source noteuspto-grants-1999_10