Hydrochloric Acid → HCID 178517825, 화합물
반응식
[O:1]([CH2:8][CH2:9][NH:10][NH2:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[ClH:12].[C:13](=[O:16])([O-])[O-].[K+].[K+].[C:19](#[N:21])C>>[O:1]([CH2:8][CH2:9][N:10]1[C:19]([Cl:12])=[N:21][C:13]([OH:16])=[N:11]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1참가 물질
실험 절차
30.4 g (0.2 mole) of 2-phenoxyethylhydrazine were dissolved in 200 ml of anhydrous acetonitrile and 7.3 g of hydrogen chloride gas were passed in at 0° C. 32 g (0.2 mole) of N-chlorocarbonyl-isocyanide-dichloride were then added dropwise to the mixture at 15°-20° C, while cooling and stirring vigorously, and after completion of the addition, 30 g of potassium carbonate were also added. The batch was next stirred for 4 hours at room temperature, in the course of which the temperature in the reaction vessel at times rose to as much as 45° C, and was then heated under reflux until no further evolution of hydrogen chloride was detectable (4-6 hours). After cooling, the residue was filtered off and washed with acetonitrile, and the total filtrate was evaporated under reduced pressure. The crystalline residue was recrystallized from a little ethanol. 21 g (43.8% of theory) of 1-(2-phenoxyethyl)-5-chloro-3-hydroxy-1,2,4-triazole of melting point 166° C were obtained. ##STR100##
후처리
- customwere passed in at 0° C
- temperaturewhile cooling
- additionwere also added
- stirringThe batch was next stirred for 4 hours at room temperature, in the course of which the temperature in the reaction vessel at times
- customrose to as much as 45° C
- temperaturewas then heated
- custom(4-6 hours)
- temperatureAfter cooling
- filtrationthe residue was filtered off
- washwashed with acetonitrile
- customthe total filtrate was evaporated under reduced pressure
- customThe crystalline residue was recrystallized from a little ethanol
출처 및 근거
- ORD 기록
- ord-c3a0a818aa454d1ba9ae32cdd076a56b
- 출처 데이터셋
- uspto-grants-1978_03
- 특허 번호
- US04081535
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