Methanol → 2,3-Difluoro-6-(hydroxymethyl)phenol
反応式
[F:1][C:2]1[C:3]([OH:12])=[C:4]([CH:8]=[CH:9][C:10]=1[F:11])[C:5](O)=[O:6].S(C)C.CO>C1COCC1>[F:1][C:2]1[C:10]([F:11])=[CH:9][CH:8]=[C:4]([CH2:5][OH:6])[C:3]=1[OH:12]参加物
5
実験手順
To a solution of 3,4-difluoro-2-hydroxy benzoic acid (3.2 g 18.39 mmol) in THF (20 mL) was added BH3.Me2S (7 mL 73.56 mmol) drop wise, over a period of 20 min. at RT. The reaction mixture was stirred at RT for 3 h and monitored by TLC. Methanol (20 mL) was added and the solvent was removed under vacuum. The crude compound was purified by column chromatography over silica gel using a mixture of ethyl acetate and hexane (20:80) as eluent to give the alcohol (2.7 g, 91% yield) MS: m/z 159 (M+1).
後処理
- customthe solvent was removed under vacuum
- customThe crude compound was purified by column chromatography over silica gel using
- additiona mixture of ethyl acetate and hexane (20:80) as eluent
出典と根拠
- ORDレコード
- ord-a2feb40b64ad4e109c672ebbd701c6e6
- 出典データセット
- uspto-grants-2011_03
- 特許番号
- US07902394B2
反応ノート
読み込み中…