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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369660Generated: November 1, 2026

Ammonium Hydroxide → 3-(Benzyl)benzamide

https://huagongshe.com/reaction/1369660

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 numberUS06579867B2
Source datasetuspto-grants-2003_06
ORD IDord-181bf77a34654f13b067b48e548c327a
Source noteuspto-grants-2003_06