1-(3-Chloro-4-methoxyphenyl)-4-methylpent-2-yne-1,4-diol → 1-(3-Chloro-4-methoxyphenyl)-4-hydroxy-4-methylpent-2-yn-1-one
反応式
[Cl:1][C:2]1[CH:3]=[C:4]([CH:10]([OH:17])[C:11]#[C:12][C:13]([CH3:16])([OH:15])[CH3:14])[CH:5]=[CH:6][C:7]=1[O:8][CH3:9]>C(Cl)Cl.O>[Cl:1][C:2]1[CH:3]=[C:4]([C:10](=[O:17])[C:11]#[C:12][C:13]([OH:15])([CH3:14])[CH3:16])[CH:5]=[CH:6][C:7]=1[O:8][CH3:9]参加物
4
実験手順
To a stirred solution of 1-(3-chloro-4-methoxyphenyl)-4-methylpent-2-yne-1,4-diol (0.69 g, 2.716 mmol) in DCM (20 mL) was added DMP (2.36 g, 5.430 mmol) at RT. The reaction mixture was stirred for 1 h and diluted with water (10 mL). The combined organic layers were washed with a saturated NaHCO3 solution and water, dried over Na2SO4, filtered, and then concentrated in vacuo to afford 1-(3-chloro4-methoxyphenyl)-4-hydroxy-4-methylpent-2-yn-1-one (0.45 g, 65%) as a brown oil.
後処理
- washThe combined organic layers were washed with a saturated NaHCO3 solution and water
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-ff0426b9660f441c82c232507112d53a
- 出典データセット
- uspto-grants-2016_02
- 特許番号
- US09265767B2
反応ノート
読み込み中…