4-Nitrophenol → HCID 178520521, 화합물
반응식
S(Cl)(Cl)=O.[CH:5]1[C:10]([N+:11]([O-:13])=[O:12])=[CH:9][CH:8]=[C:7]([OH:14])[CH:6]=1.[CH:15]1[N:19]=[CH:18][NH:17][C:16]=1/[CH:20]=[CH:21]/[C:22](O)=[O:23].[Cl-].[Cl-].[Ca+2]>>[NH:19]1[CH:15]=[C:16](/[CH:20]=[CH:21]/[C:22]([O:14][C:7]2[CH:8]=[CH:9][C:10]([N+:11]([O-:13])=[O:12])=[CH:5][CH:6]=2)=[O:23])[N:17]=[CH:18]1참가 물질
실험 절차
2 ml (27.5 mmol) of freshly distilled thionyl chloride are added to a finely ground mixture of 1.51 g (10.8 mmol) of p-nitrophenol and 1.5 g (10.8 mmol) of trans-urocanic acid in a round-bottomed flask equipped with a drying tube containing CaCl2. The mixture is progressively brought to 140° C. After 4 h, the mixture is slowly cooled to room temperature. A brown powder is extracted with CHCl3 / MeOH (150 ml, 2:1) while heating. The undissolved material is separated by filtration and the filtrate is treated with active charcoal. Concentration is carried out under vacuum and diethyl ether is added so as to induce precipitation of a solid (1.96 g; overall crude yield: 61%). The latter is recrystallized from MeOH and the product is washed with diethyl ether in order to remove any trace of p-nitrophenol, giving a crystalline white solid, M.p. 220°-222° C.
후처리
- customequipped with a drying tube
- customis progressively brought to 140° C
- extractionA brown powder is extracted with CHCl3 / MeOH (150 ml, 2:1)
- temperaturewhile heating
- customThe undissolved material is separated by filtration
- additionthe filtrate is treated with active charcoal
- concentrationConcentration
- additionis added so as
- customprecipitation of a solid (1.96 g; overall crude yield: 61%)
- customThe latter is recrystallized from MeOH
- washthe product is washed with diethyl ether in order
- customto remove any trace of p-nitrophenol
- customgiving a crystalline white solid, M.p. 220°-222° C.
출처 및 근거
- ORD 기록
- ord-095cfbd09e5547f2aa2289eba12c92fc
- 출처 데이터셋
- uspto-grants-1998_01
- 특허 번호
- US05708171
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