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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258452Generated: November 2, 2026

Sodium hydride → N-[2-(Benzyloxy)-4-bromo-6-nitrophenyl]-N-(2-methoxyethyl)acetamide

https://huagongshe.com/reaction/1258452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Bromoethyl methyl etherHCID 80972—
ReactantN-(2-(benzyloxy)-4-bromo-6-nitrophenyl)acetamideHCID 67220372—
SolventDimethylformamideHCID 6228—
ProductN-[2-(Benzyloxy)-4-bromo-6-nitrophenyl]-N-(2-methoxyethyl)acetamideHCID 6722053377.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of sodium hydride (60% dispersion in mineral oil, 1.78 g, 44.5 mmol) in N,N-dimethylformamide (100 mL) was added dropwise a solution of N-[2-(benzyloxy)-4-bromo-6-nitrophenyl]acetamide (13.5 g, 37.1 mmol, Step 1) in N,N-dimethylformamide at 0° C. over 10 minutes. After stirring at 0° C. for 20 minutes, 1-bromo-2-methoxyethane (7.21 g, 51.9 mmol) was added, and the mixture was stirred at 50° C. for 2 hours. After cooling to room temperature, the mixture was poured onto water, and the aqueous layer was extracted with ethyl acetate/toluene (3:1). The combined organic layer was dried over magnesium sulfate and concentrated in vacuo. The residue was purified by column chromatography on silica gel eluting with hexane/ethyl acetate (3:1) to afford the title compound as a gray solid (12.1 g, 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466166B2
Source datasetuspto-grants-2013_06
ORD IDord-2ffddae088974f23986f8611e078d108
Source noteuspto-grants-2013_06