反応式
ClC12[O:8]C1CCC(Cl)(F)C2.[CH3:11][C:12]1(O)[C:17]([Cl:19])([Cl:18])[CH2:16][CH2:15][CH2:14][C:13]1([Cl:21])Cl.[OH-].[Na+]>O>[Cl:21][C:13]12[O:8][CH:14]1[CH2:15][CH2:16][C:17]([Cl:19])([Cl:18])[CH:12]2[CH3:11]参加物
5
実験手順
The same procedure was employed as for the preparation of 2e in Example 17: it was performed with 3.97 g (15.75 mmol) of crude alcohol 1j, 20 cm3 of distilled water and 2.4 g (60 mmol) of sodium hydroxide; reaction time was 1 h 15 min; ether extraction (5×40 cm3); 3.29 g of epoxide 2h were obtained having a 95.5% yield based on the ketone (macrobore GC purity>99%)
後処理
- customreaction time
- extractionether extraction (5×40 cm3)
出典と根拠
- ORDレコード
- ord-fa28d522f0fe44109c518a5623e6ed9b
- 出典データセット
- uspto-grants-1998_10
- 特許番号
- US05817890
関連ノート
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