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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433363Generated: October 29, 2026

Ammonium Hydroxide → 3-(Benzyl)benzamide

https://huagongshe.com/reaction/433363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantOxalyl chlorideHCID 65578—
Reactant3-Benzylbenzoic acidHCID 4124553—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product3-(Benzyl)benzamideHCID 22238827—

Reaction Steps

To the product from Step A (0.0119 moles) was added 150 mL of CH2Cl2, one drop of DMF, 10 mL of oxalyl chloride, and the mixture was stirred at room temperature for 3 hours. After cooling to 10° C., 30 mL of NH4OH (exothermic) was added and the mixture was stirred for 30 min. The reaction mixture was then concentrated and the resulting residue diluted with ethyl acetate. The organic layer was washed with 1N NaOH, brine, dried over Na2SO4, and concentrated to give the 3-(benzyl)benzamide as a white solid, which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06667305B1
Source datasetuspto-grants-2003_12
ORD IDord-a1181be573d74d35ae4a39e524756ba4
Source noteuspto-grants-2003_12