HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401135Generated: October 25, 2026
Bromobenzene → 1-Phenyl-2-(thiophen-3-yl)ethanone
https://huagongshe.com/reaction/401135
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | N-methoxy-N-methyl-2-(thiophen-3-yl)acetamide | HCID 11423995 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Phenyl-2-(thiophen-3-yl)ethanone | HCID 12233113 | 55% |
Reaction Steps
To the solution of bromo-benzene (1.0 g, 6.36 mmol) in anhydrous THF (30 mL) was added n-BuLi (5.9 mmol, 2.4 mL) at −78° C. under nitrogen, and the mixture was stirred at −78° C. for further 20 min., a solution of N-methoxy-N-methyl-2-(thiophen-3-yl)acetamide (1 g, 5.4 mmol) in anhydrous THF (10 mL) was added. The resulting mixture was stirred at −78° C. under nitrogen for about 30 min., poured into NH4Cl aqueous solution, and extracted with EtOAc. The organic layers were washed with brine, dried over sodium sulfate, concentrated, and purified by column chromatograph (PE:EtOAc=20:1) to afford Intermediate 2 as a colorless oil (600 mg, yield 55.0%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08741915B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-a89dfd87cb0842c393f81dc108631a7c |
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| Source note | uspto-grants-2014_06 |
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