Oxalyl chloride → HCID 19016259、化合物
反応式
[CH3:1][O:2][C:3]1[CH:11]=[CH:10][C:6]([C:7](O)=[O:8])=[CH:5][C:4]=1[O:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26].C(Cl)(=O)C([Cl:30])=O>C(Cl)Cl.CN(C)C=O>[CH3:1][O:2][C:3]1[CH:11]=[CH:10][C:6]([C:7]([Cl:30])=[O:8])=[CH:5][C:4]=1[O:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26]参加物
5
実験手順
To a mixture of 50 g of product from Example 42 in 500 ml of methylene chloride and 15 drops of dimethylformamide is added, dropwise, 26.12 g of oxalyl chloride. The reaction is stirred at room temperature for 18 hours and concentrated in vacuo. The residue is recrystallized from diethyl ether to give 52.3 g of the desired product as white crystals.
後処理
- additionis added
- concentrationconcentrated in vacuo
- customThe residue is recrystallized from diethyl ether
出典と根拠
- ORDレコード
- ord-6c0c6d8358fe49dcbbf6c8d77e91340f
- 出典データセット
- uspto-grants-1993_05
- 特許番号
- US05208247
反応ノート
読み込み中…