HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351749Generated: October 25, 2026
2-Acetyl-5-bromothiophene → 5-Bromo-alpha,alpha-dimethyl-2-thiophenemethanol
https://huagongshe.com/reaction/351749
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Acetyl-5-bromothiophene | HCID 79335 | — |
| Reactant | Tetrahydrofuran toluene | HCID 22635083 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Bromo-alpha,alpha-dimethyl-2-thiophenemethanol | HCID 22714302 | — |
Reaction Steps
To a solution of 2-acetyl-5-bromothiophene in THF (2.5 mL/mmol) at −30° C. was added 1.4M methylmagnesium bromide in 3:1 toluene-THF (1.5 eq) and the resulting mixture was warmed to −10° C. and stirred for 1.5 hours. After quenching with saturated aqueous ammonium chloride solution, the mixture was partitioned between ether and water. The organic fraction was dried and evaporated, and the crude material was chromatographed on silica gel eluting with a 1:4 mixture of ether and hexane to afford the 2-bromo-5-(1-hydroxy-1-methylethyl)thiophene compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06743802B2 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-1e0a865ae353492d95932dc9687937af |
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| Source note | uspto-grants-2004_06 |
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