Diethyl Ether → 2-Benzofuran-3-yl-ethanol
反応式
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]=12参加物
4
実験手順
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%).
後処理
- 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%)
出典と根拠
- ORDレコード
- ord-59bad4e82581494b96c626227b667a12
- 出典データセット
- uspto-grants-2010_08
- 特許番号
- US07776848B2
反応ノート
読み込み中…