Hydrogen Bromide → 2-[4,5-Bis-(p-methoxyphenyl)-thiazol-2-ylthio]-acetaldehyde
반응식
C([O:3][C:4](=O)[CH:5]([S:8][C:9]1[S:10][C:11]([C:22]2[CH:27]=[CH:26][C:25]([O:28][CH3:29])=[CH:24][CH:23]=2)=[C:12]([C:14]2[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[CH:16][CH:15]=2)[N:13]=1)C=O)C.Br>C(O)(=O)C>[CH3:21][O:20][C:17]1[CH:18]=[CH:19][C:14]([C:12]2[N:13]=[C:9]([S:8][CH2:5][CH:4]=[O:3])[S:10][C:11]=2[C:22]2[CH:27]=[CH:26][C:25]([O:28][CH3:29])=[CH:24][CH:23]=2)=[CH:15][CH:16]=1참가 물질
4
실험 절차
4.0 g of 2-[4,5-bis-(p-methoxyphenyl)-thiazol-2-ylthio]-2-formylacetic acid ethyl ester are dissolved in 50 ml of acetic acid, 10 ml of 43% strength hydrobromic acid are added and the mixture is heated at 80° for 4 hours. The mixture is concentrated to dryness by evaporation under reduced pressure, and the residue is dissolved in 200 ml of ethyl acetate, washed twice with 50 ml of saturated sodium bicarbonate solution each time and with water, dried over magnesium sulphate and concentrated to dryness by evaporation. The crude product is recrystallised from hexane/diethyl ether (55 ml+10 ml). 2-[4,5-bis-(p-methoxyphenyl)-thiazol-2-ylthio]-acetaldehyde having a melting point of 75°-76° is obtained.
후처리
- temperaturethe mixture is heated at 80° for 4 hours
- concentrationThe mixture is concentrated to dryness by evaporation under reduced pressure
- dissolutionthe residue is dissolved in 200 ml of ethyl acetate
- washwashed twice with 50 ml of saturated sodium bicarbonate solution each time
- dry with materialwith water, dried over magnesium sulphate
- concentrationconcentrated to dryness by evaporation
- customThe crude product is recrystallised from hexane/diethyl ether (55 ml+10 ml)
출처 및 근거
- ORD 기록
- ord-7cae3f533ddd46688009f0690d0c1218
- 출처 데이터셋
- uspto-grants-1984_05
- 특허 번호
- US04451471
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