Methyl chloroformate → HCID 178502040、化合物
反応式
S(O)(O)(=O)=O.CS[C:8](=[NH:10])[NH2:9].Cl[C:12]([O:14][CH3:15])=[O:13].[OH-].[Na+].[Cl:18][C:19]1([Cl:32])[CH2:21][CH:20]1[CH2:22][S:23][C:24]1[CH:29]=[CH:28][C:27]([NH2:30])=[C:26](N)[CH:25]=1>O.CO.C(O)(=O)C>[Cl:32][C:19]1([Cl:18])[CH2:21][CH:20]1[CH2:22][S:23][C:24]1[CH:29]=[CH:28][C:27]2[NH:30][C:8]([NH:9][C:12](=[O:13])[O:14][CH3:15])=[N:10][C:26]=2[CH:25]=1参加物
8
実験手順
To a mixture of 9 g of 2-methyl-2-thiopseudourea sulfate in 6 ml of H2O there is added 5.7 ml of methyl chloroformate at 0° C. and the mixture is stirred for 15 minutes. Then there is added 12 ml of 25% NaOH dropwise and the mixture is stirred for 15 minutes. Then there is added 6 ml of acetic acid dropwise and the mixture is stirred for 15 minutes. Then the total amount of 4-[(2,2-dichlorocyclopropyl)methyl]thio-o-phenylenediamine from above in 50 ml of methanol is added and the mixture is refluxed for 2 hours. The alcohol is removed in vacuo and H2O is added. The resulting solid is filtered off and cyystallized from glyme to yield 5.4 g, m.p. 211°-213°.
後処理
- stirringthe mixture is stirred for 15 minutes
- stirringthe mixture is stirred for 15 minutes
- temperaturethe mixture is refluxed for 2 hours
- customThe alcohol is removed in vacuo and H2O
- additionis added
- filtrationThe resulting solid is filtered off
- customto yield 5.4 g, m.p. 211°-213°
出典と根拠
- ORDレコード
- ord-60d8b7dd85d8491692b2a239cab8489c
- 出典データセット
- uspto-grants-1982_07
- 特許番号
- USRE030990
反応ノート
読み込み中…