반응식
[C:1]([N:4]1[CH2:13][CH2:12][C:11]2[C:6](=[C:7](N)[C:8]([Cl:14])=[CH:9][CH:10]=2)[CH2:5]1)(=[O:3])[CH3:2].N([O-])=O.[Na+].N(O)=O.[Cl-:23].[Mg+2].[Cl-].[S:26](=[O:28])=[O:27]>Cl.O.C(O)(=O)C>[C:1]([N:4]1[CH2:13][CH2:12][C:11]2[C:6](=[C:7]([S:26]([Cl:23])(=[O:28])=[O:27])[C:8]([Cl:14])=[CH:9][CH:10]=2)[CH2:5]1)(=[O:3])[CH3:2]참가 물질
반응물 5
생성물 1
시약·촉매·용매 3
반응 조건
- 온도
- 30 °C
실험 절차
2-Acetyl-8-amino-7-chloro-1,2,3,4-tetrahydroisoquinoline (0.04 mole) in concentrated hydrochloric acid (8.4 ml.) is cooled to 3° C. and treated with sodium nitrite (0.044 mole) dissolved in water (6 ml.). After stirring for 30 minutes, the reaction is tested for nitrous acid with starch/iodide paper. If the test for nitrous acid is negative, more sodium nitrite is added in small portions with stirring over a period of time until the test is positive. When a positive reaction is obtained, magnesium chloride (0.032 mole) is added and the resulting mixture is added to a mixture of acetic acid (40 ml.) saturated with sulfur dioxide and cuprous chloride dihydrate (0.0129 mole) maintained at 30° C. and stirred. After about 30 minutes, the mixture is diluted with water (60 ml.) and extracted with ether. The extract is then washed with dilute aqueous sodium bicarbonate/sodium carbonate solution at pH 8-9, then with water, and dried over sodium sulfate. The ether is evaporated to yield 2-acetyl-8-chlorosulfonyl-7-chloro-1,2,3,4-tetrahydroisoquinoline.
후처리
- stirringwith stirring over a period of time until the test
- customWhen a positive reaction
- customis obtained
- stirringstirred
- waitAfter about 30 minutes
- extractionextracted with ether
- washThe extract is then washed with dilute aqueous sodium bicarbonate/sodium carbonate solution at pH 8-9
- dry with materialwith water, and dried over sodium sulfate
- customThe ether is evaporated
출처 및 근거
- ORD 기록
- ord-0cf1bb2f5c0b42889e527665e590cf69
- 출처 데이터셋
- uspto-grants-1976_10
- 특허 번호
- US03988339
연결된 노트
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