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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003208Generated: October 30, 2026

1,2-Dichloroethane → Benzamide

https://huagongshe.com/reaction/1003208

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantEthyl AcetateHCID 8857—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant3-Hydroxy-2-methylbenzoic AcidHCID 252023—
SolventDimethylformamideHCID 6228—
ProductBenzamideHCID 2331261.7%

Reaction Steps

To a solution of 187 mg (1.23 mmol) of 3-hydroxy-2-methylbenzoic acid and 217 mg (1.61 mmol) of N-hydroxybenzotriazole in 6 mL of anhydrous N,N-dimethylformamide at 0° C., was added 236 mg (1.23 mmol) of EDC. After 20 minutes of activation at 0° C. and 1 hour at room temperature, 450 mg (1.07 mmol) of 2R-hydroxy-3-[[(1,3-benzodioxol-5-yl)sulfonyl](2-methylpropyl)amino]-1S-(phenylmethyl)propylamine was added. After 15 hours at room temperature, ethyl acetate was added, washed with 5% citric acid, saturated sodium bicarbonate, brine, dried, filtered and concentrated to afford 650 mg of crude material. This was chromatographed on silica gel using 0-25% ethyl acetate/methylene chloride as eluent to afford 390 mg of pure benzamide, N-[2R-hydroxy-3-[[(1,3-benzodioxol-5-yl)sulfonyl](2-methylpropyl)amino]-1S-(phenylmethyl)propyl]-3-hydroxy-2-methyl, m/e=561(M+Li).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06046190
Source datasetuspto-grants-2000_04
ORD IDord-0c4accd723c14cd99cc9755bcca13f73
Source noteuspto-grants-2000_04