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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553361Generated: October 31, 2026

Triethylamine → Benzamide

https://huagongshe.com/reaction/553361

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 numberUSRE042889E1
Source datasetuspto-grants-2011_11
ORD IDord-ff2021606e9a467586392bd68832c7ae
Source noteuspto-grants-2011_11