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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298337Generated: October 29, 2026

Sodium hydride → HCID 18385687, compound

https://huagongshe.com/reaction/2298337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Bromo-2-methylpropanoyl cyanideHCID 12487838—
ReactantHCID 18385650HCID 18385650—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18385687HCID 18385687—

Reaction Steps

437 mg of 1-{3-methyl-4-(methylthio)phenyl}-2-(3-fluorophenyl)-ethanone in 50 ml dry THF was stirred with 67 mg of 60% oil dispersion of sodium hydride for an hour at 0° C., which was followed by dropwise addition of 0.8 ml α-bromoisobutyryl cyanide diluted with 25 ml THF. The reaction solution was slowly warmed to room temperature and was stirred overnight. Then the solvent was removed in vacuo and the resulting residue was extracted with 50 ml water and dichloromethane (50 ml×3). The organic layer was concentrated in vacuo and was purified by column chromatography (hexane/ethylacetate=6:1) to yield 312 mg of 2,2-dimethyl-4-(3-fluorophenyl)-5-{3-methyl-4-(methylthio)phenyl}-3(2H)-furanone. NMR: δ1.55 (s, 6H), 2.27 (s, 3H), 2.48 (s, 3H), 7.36 (m, 4H), 7.32 (m, 1H), 7.45 (m, 2H). IR 1694, 1601, 1385, 1260, 1192.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492416B1
Source datasetuspto-grants-2002_12
ORD IDord-e48ef286511b4ad996bfee0b5a1291ee
Source noteuspto-grants-2002_12