Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114177Generated: October 26, 2026

Benzyl Alcohol → 5-benzyloxy-N,N-dimethyl-2-nitrobenzamide

https://huagongshe.com/reaction/2114177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantSodium hydrideHCID 24758—
Reactant5-Chloro-N,N-dimethyl-2-nitrobenzamideHCID 22934807—
SolventDimethylformamideHCID 6228—
Product5-benzyloxy-N,N-dimethyl-2-nitrobenzamideHCID 2313026789.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium hydride (210 mg) was suspended in DMF (10 mL), and the suspension was cooled to 0° C. and thereto were added benzyl alcohol (568 mg) and a solution of 5-chloro-N,N-dimethyl-2-nitrobenzamide (1.00 g) in DMF (2 mL). The mixture was stirred at 50° C. for 0.5 hour and then concentrated. The residue was acidified with 2N hydrochloric acid and extracted with ethyl acetate. The extract was washed with water and concentrated. The residue was purified by column chromatography on silica gel (ethyl acetate:hexane=1:2→2:3) to give 5-benzyloxy-N,N-dimethyl-2-nitrobenzamide (1.18 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432392B2
Source datasetuspto-grants-2008_10
ORD IDord-fc65824a0cfa40f8a7587440764e6c86
Source noteuspto-grants-2008_10