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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454220Generated: October 31, 2026

Sodium → 1-(2-Fluoro-3-methoxy-6-nitrophenyl)propan-2-one

https://huagongshe.com/reaction/454220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodiumHCID 5360545—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 22030751HCID 22030751—
SolventMethanolHCID 887—
Product1-(2-Fluoro-3-methoxy-6-nitrophenyl)propan-2-oneHCID 2203074390%

Reaction Conditions

Temperature5 °C

Reaction Steps

A solution of sodium methoxide (freshly prepared from sodium (1.71 g) and methanol (35 ml)) was added to a solution of 1,2-difluoro-3-(2,2-dimethoxypropyl)-4-nitrobenzene (16.2 g, 62 mmol), (prepared as described above), in methanol (200 ml) cooled at 5° C. The mixture was left to warm to ambient temperature and was stirred for 3 days. The volatiles were removed under vacuum and the residue was partitioned between ethyl acetate and 2N hydrochloric acid (1 ml). The organic layer was concentrated to a total volume of 100 ml and THF (100 ml) and 6N hydrochloric acid (25 ml) were added. The mixture was stirred for 1 hour at ambient temperature. The volatiles were removed under vacuum and the residue was partitioned between ethyl acetate and water. The organic layer was separated, washed with water, brine, dried (MgSO4) and evaporated. The residue was purified by column chromatography eluting with ethyl acetate/petroleum ether (3/7) to give 3-acetylmethyl-2-fluoro-1-methoxy-4-nitrobenzene (12.7 g, 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492560B2
Source datasetuspto-grants-2013_07
ORD IDord-9442689db3e0417b98736ee3f4ee3471
Source noteuspto-grants-2013_07