참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Acetyl-5-bromothiophene | HCID 79335 | — |
| 반응물 | Tetrahydrofuran toluene | HCID 22635083 | — |
| 반응물 | HCID 178418573 | HCID 178418573 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 5-Bromo-alpha,alpha-dimethyl-2-thiophenemethanol | HCID 22714302 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06743802B2 |
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| 출처 데이터셋 | uspto-grants-2004_06 |
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| ORD ID | ord-1e0a865ae353492d95932dc9687937af |
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| 출처 메모 | uspto-grants-2004_06 |
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