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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241356Generated: October 27, 2026

2-Fluoro-1-phenylethan-1-one → Methyl 3-methylbenzo[b]thiophene-2-carboxylate

https://huagongshe.com/reaction/241356

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-1-phenylethan-1-oneHCID 9947—
ReactantMethyl ThioglycolateHCID 16907—
ReactantSodium hydrideHCID 24758—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-methylbenzo[b]thiophene-2-carboxylateHCID 26865836%

Reaction Steps

To a suspension of 55% sodium hydride (390 mg, 9.69 mmol) in THF (7 mL)-DMSO (20 mL) was added methyl thioglycolate (0.64 ml) under N2 atmosphere. After ceasing of bubbling, the mixture was stirred for 15 minutes at room temperature, to which was added slowly a solution of 2-fluoroacetophenone (0.89 mL, 6.46 mmol) in DMSO (5 mL). The mixture was stirred at room temperature for 1 hour, diluted with water, and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure, and the residue was recrystallized from ethyl acetate/hexane to give the titled compound as a white crystal (533 mg, 36%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648208B2
Source datasetuspto-grants-2014_02
ORD IDord-85fd540bcc394a2ab65a26be9ede688e
Source noteuspto-grants-2014_02