Diethyl Ether → 2-Benzofuran-3-yl-ethanol
반응식
CO[C:3](=O)[CH2:4][C:5]1[C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=2[O:7][CH:6]=1.[Li].CC[O:18]CC>>[CH:6]1[O:7][C:8]([CH:13]([OH:18])[CH3:12])=[C:9]2[CH:10]=[CH:11][CH:3]=[CH:4][C:5]=12참가 물질
4
실험 절차
A solution of benzofuran-3-yl-acetic acid methyl ester (4.0 g, 21 mmol) in 25 ml of ether was added dropwise at RT to a suspension of lithium alanate (1.61 g, 59.5 mmol) in 35 ml of ether, and stirring was then carried out for 30 minutes. Excess alanate was then hydrolysed with ethanol, the mixture was suction-filtered over Kieselguhr, and the solvent was removed in vacuo. The product was obtained in the form of a yellowish oil in a yield of 3.0 g (89%).
후처리
- filtrationhydrolysed with ethanol, the mixture was suction-filtered over Kieselguhr
- customthe solvent was removed in vacuo
- customThe product was obtained in the form of a yellowish oil in a yield of 3.0 g (89%)
출처 및 근거
- ORD 기록
- ord-59bad4e82581494b96c626227b667a12
- 출처 데이터셋
- uspto-grants-2010_08
- 특허 번호
- US07776848B2
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