반응식
[C:1]1([NH:7][C:8](=S)[NH:9][NH2:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl.Cl[CH2:14][C:15]([CH2:17][C:18](=O)[CH3:19])=[O:16]>O1CCCC1>[NH:7]([C:8]1[C:17]([C:15](=[O:16])[CH3:14])=[C:18]([CH3:19])[NH:10][N:9]=1)[C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1참가 물질
5
실험 절차
50 g of 4-phenylthiosemicarbazide is suspended in 300 ml of tetrahydrofuran and 0.5 ml of concentrated HCl is added. Then 40.4 g of 3-chloroacetyl acetone is allowed to run in all at once and the whole is cooled with an ice-bath. After 12 hours' stirring, the precipitate formed is suction filtered, washed with acetone and then boiled in a water/acetone mixture (1:1). This hot solution is filtered off from the sulfur and neutralized with aqueous ammonia solution. The product is then suction filtered and recrystallized from acetone; m.p. 246°-247° C.
후처리
- temperatureis cooled with an ice-bath
- customthe precipitate formed
- filtrationfiltered
- washwashed with acetone
- filtrationThis hot solution is filtered off from the sulfur and neutralized with aqueous ammonia solution
- filtrationsuction filtered
- customrecrystallized from acetone
출처 및 근거
- ORD 기록
- ord-6e8d420a9d6449bca3b577d317c15304
- 출처 데이터셋
- uspto-grants-1981_04
- 특허 번호
- US04260775
연결된 노트
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