참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Aluminium lithium hydride | HCID 21226445 | — |
| 반응물 | Benzyl 4,4,4-trifluoro-3-methylbut-2-enoate | HCID 66705445 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | 4,4,4-Trifluoro-3-methylbut-2-en-1-ol | HCID 54043180 | — |
반응 단계
Benzyl 4,4,4-trifluoro-3-methylbut-2-enoate (1.87 g, 7.67 mmol) in diethyl ether (5 mL) was added dropwise to a suspension of LAH (291 mg, 1.67 mmol) in diethyl ether (10 mL). After stirring at −78° C. for 10 min and at 0° C. for a further 30 min, the reaction mixture was filtered through cotton, quenched with sodium potassium tartrate and stirred vigorously until layers separated. The aqueous phase was extracted with diethyl ether. The combined ethereal layers were dried (magnesium sulfate) and concentrated in vacuo to afford 4,4,4-trifluoro-3-methylbut-2-en-1-ol which was used in the subsequent step without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US08106070B2 |
|---|
| 출처 데이터셋 | uspto-grants-2012_01 |
|---|
| ORD ID | ord-60e6decf846e40219145f8431dee51c9 |
|---|
| 출처 메모 | uspto-grants-2012_01 |
|---|