7,8-difluoro-2-pentyl-2H-chromene → 7,8-Difluoro-2-pentyl-3,4-dihydro-2H-1-benzopyran
反応式
[F:1][C:2]1[C:11]([F:12])=[C:10]2[C:5]([CH:6]=[CH:7][CH:8]([CH2:13][CH2:14][CH2:15][CH2:16][CH3:17])[O:9]2)=[CH:4][CH:3]=1>C1(C)C=CC=CC=1.[Pd]>[F:1][C:2]1[C:11]([F:12])=[C:10]2[C:5]([CH2:6][CH2:7][CH:8]([CH2:13][CH2:14][CH2:15][CH2:16][CH3:17])[O:9]2)=[CH:4][CH:3]=1参加物
4
実験手順
51.0 g (0.21 mol) of 7,8-difluoro-2-pentyl-2H-chromene are hydrogenated for 1 h at room temperature in 510 ml of toluene in the presence of Pd/C (5% Pd). The batch is concentrated to dryness. The crude product (yellowish liquid) can be used directly for the next step.
後処理
- concentrationThe batch is concentrated to dryness
出典と根拠
- ORDレコード
- ord-ca755439fb5045dcb9ae84d32c68a691
- 出典データセット
- uspto-grants-2010_03
- 特許番号
- US07678929B2
反応ノート
読み込み中…