Benzyl 3,3-difluorocyclobutane-1-carboxylate → 3,3-Difluorocyclobutane-1-carboxylic acid
反応式
[F:1][C:2]1([F:16])[CH2:5][CH:4]([C:6]([O:8]CC2C=CC=CC=2)=[O:7])[CH2:3]1>C(O)C.[Pd]>[F:1][C:2]1([F:16])[CH2:5][CH:4]([C:6]([OH:8])=[O:7])[CH2:3]1参加物
4
実験手順
To a solution of benzyl 3,3-difluorocyclobutanecarboxylate (1.4 g, 6.2 mmol) in ethanol (50 mL) was added palladium on activated carbon (500 mg) and the reaction mixture was stirred at RT under an atmosphere of hydrogen (1 atm) for 12 h. The reaction mixture was filtered through a pad of CELITE® and the filtrate was concentrated to afford Intermediate 291A as pale yellow liquid (550 mg, 65% yield). 1H NMR (400 MHz, DMSO-d6) δ ppm 12.97-12.76 (m, 1H), 3.04-2.91 (m, 1H), 2.89-2.64 (m, 4H).
後処理
- filtrationThe reaction mixture was filtered through a pad of CELITE®
- concentrationthe filtrate was concentrated
出典と根拠
- ORDレコード
- ord-a3d70355b97948f4a5658a443bdef9b6
- 出典データセット
- uspto-grants-2016_03
- 特許番号
- US09273058B2
反応ノート
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