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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683503Generated: October 30, 2026

Sodium Hydroxide → 7-Fluoro-8-methyl-5-nitro-3,4-dihydronaphthalen-1(2H)-one

https://huagongshe.com/reaction/1683503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 4-(4-fluoro-5-methyl-2-nitrophenyl)butanoateHCID 22449411—
SolventMethanolHCID 887—
Product7-Fluoro-8-methyl-5-nitro-3,4-dihydronaphthalen-1(2H)-oneHCID 22449406—

Reaction Steps

The compound obtained in (3) above (7.1 gm) was dissolved in 20 ml of methanol. To the solution was added 10 ml of 15% aqueous solution of sodium hydroxide and the mixture was stirred for 3 hours at room temperature. The reaction mixture was concentrated, acidified with concentrated hydrochloric acid, and extracted with chloroform. The chloroform layer was washed with water and saturated brine in this order and dried over anhydrous sodium sulfate. The solvent was evaporated, and the residue was slowly added to 50 ml of polyphosphoric acid heated to 110° C. and stirred for 4.5 hours. After the addition of 100 ml of ice-water, the reaction product was extracted with ethyl acetate, washed with water, saturated sodium bicarbonate and saturated brine in this order, and dried over anhydrous sodium sulfate. The solvent was evaporated, and the residue was subjected to silica gel column chromatography using a hexane-ethyl acetate (1:1) mixed solvent as an eluant to obtain fractions containing the target compound. The fractions were concentrated to produce 1.7 gm of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05637770
Source datasetuspto-grants-1997_06
ORD IDord-c0c0248c0439485f98bdaa88be3548c1
Source noteuspto-grants-1997_06