HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862732Generated: October 26, 2026
2-Methylthiophene → 1-(5-Methyl-thien-2-yl)3,4-dihydro-4,4-dimethyl-7-bromo-naphthalene
https://huagongshe.com/reaction/1862732
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methylthiophene | HCID 11126 | — |
| Reactant | 7-Bromo-4,4-dimethyl-1,2,3,4-tetrahydronaphthalen-1-one | HCID 10753357 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Diethylether ethylacetate | HCID 21584169 | — |
| Product | 1-(5-Methyl-thien-2-yl)3,4-dihydro-4,4-dimethyl-7-bromo-naphthalene | HCID 18620062 | 62.3% |
Reaction Steps
To a cold (−78° C.) solution of 2-methylthiophene (800 mg, 8.1 mmol) in THF (10 mL) was added n-BuLi (1.6M solution in hexane, 5 mL). The mixture was stirred for 1.5 hours and transferred to a cold (−78° C.) flask containing 3,4-dihydro-4,4-dimethyl-7-bromo-1(2H)-naphthalenone (Compound A, 1.63 g, 6.5 mmol), in THF (15 mL). The mixture was gradually warmed to 0° C. The reaction mixture was diluted with ether:ethylacetate (1:1, 80 mL), washed with water (10 mL), brine (10 mL), dried with MgSO4 and the solvent was removed by evaporation. The crude material was dissolved in dichloroethane (20 mL) and pTSA (40 mg) was added. The mixture was stirred at ambient temperature for 16 hours and at 50° C. for 4 hours. The reaction mixture was diluted with ether (150 mL), washed with aqueous 10% NaHCO3 (10 mL), brine (10 mL) and dried with MgSO4. Purification by chromatography on silica gel gave 1.35 g of the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06538149B1 |
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| Source dataset | uspto-grants-2003_03 |
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| ORD ID | ord-db1baf09c31e4b26bae399fd6806fe09 |
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| Source note | uspto-grants-2003_03 |
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