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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2623Generated: October 26, 2026

2-Methylthiophene → 2,2-Dimethyl-4(2-methyl-thien-5-yl)-6-bromo-thiochrom-3-ene

https://huagongshe.com/reaction/2623

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylthiopheneHCID 11126—
Reactant6-Bromo-2,2-dimethylthiochroman-4-oneHCID 22218317—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product2,2-Dimethyl-4(2-methyl-thien-5-yl)-6-bromo-thiochrom-3-eneHCID 86191489—

Reaction Steps

To a cold (-78° C.) solution of 2-methylthiophene (1.2 g, 12.2 mmol) in THF (8 mL) was added n-BuLi in hexane (1.6M, 8.5 mL). The mixture was warmed to ambient temperature over 30 minutes. with stirring. The mixture was recooled to -78° C. and a solution of 2,2-dimethyl-6-bromo-thiochroman-4-one (Compound M, 1.4 g, 5.2 mmol) in THF (10 mL) was added. The mixture was stirred for 16 hours at ambient temperature. Then the reaction mixture was diluted with ether (125 mL), washed with water (10 mL), brine (10 mL) dried and the solvent was removed by evaporation. The product was seperated by column chromatography and was dissolved in dichloromethane (5 mL). To this solution p-TSA (5 mg) was added and the mixture was stirred at ambient temperature for 5 min. The reaction was quenched with 10% NaHCO3 (3 mL), washed with brine (5 mL), dried and the solvent was removed by distillation. The residual crude material was purified by column chromatography to obtain the title compound as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05728846
Source datasetuspto-grants-1998_03
ORD IDord-4ced6f59ef644dca80ccd38e6f9bbbd4
Source noteuspto-grants-1998_03