HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288316Generated: October 26, 2026
2-Methylthiophene → 2,2-Dimethyl-4(2-methyl-thien-5-yl)-6-bromo-thiochrom-3-ene
https://huagongshe.com/reaction/2288316
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methylthiophene | HCID 11126 | — |
| Reactant | 6-Bromo-2,2-dimethylthiochroman-4-one | HCID 22218317 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2,2-Dimethyl-4(2-methyl-thien-5-yl)-6-bromo-thiochrom-3-ene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06087505 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-fd6529114f5948c99baa2cd1d4b7768a |
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| Source note | uspto-grants-2000_07 |
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