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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037660Generated: October 26, 2026

Benzyl Chloride → 2-(Benzyloxy)-N,N-dimethylbenzamide

https://huagongshe.com/reaction/1037660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Hydroxy-N,N-dimethylbenzamideHCID 74500—
SolventDimethylformamideHCID 6228—
Product2-(Benzyloxy)-N,N-dimethylbenzamideHCID 13073602—

Reaction Steps

In an argon atmosphere, a mixture of 6.55 g (39.7 mmol) of 15, 10.9 g (79.3 mmol) of K2CO3, 1.0 g (5.94 mmol) of KI and 80 mL of anhydrous DMF was stirred for 10 min at room temperature. After that 7.52 g (59.5 mmol) of benzyl chloride was added in one portion. The resulting mixture was stirred for 2 hr at 70° C. and then evaporated to dryness. To the residue, 70 mL of water and 30 mL of dichloromethane were added. The organic layer was separated, and the aqueous layer was washed by 2×50 mL of dichloromethane. The combined organic extract was dried over Na2SO4 and then evaporated to dryness. The residue was washed by 50 mL of cold ether and dried in vacuum. Yield 9.71 g (96%) of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546501B2
Source datasetuspto-grants-2013_10
ORD IDord-21dbb1cece184c71aed5c3aeab22a8fa
Source noteuspto-grants-2013_10