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[CH3:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[N+:11]([O-:13])=[O:12])[C:5]([OH:7])=[O:6].[CH3:14]O>>[CH3:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[N+:11]([O-:13])=[O:12])[C:5]([O:7][CH3:14])=[O:6]참가 물질
3
실험 절차
In a 5-liter three-necked round-bottomed flask equipped with a reflux condenser, overhead stirrer and gas inlet, was placed 300 g of 3-methyl-4-nitrobenzoic acid and 3 l of methanol. To the resulting well-stirred solution was bubbled in 20.8 g of hydrogen chloride and the resulting mixture was refluxed for 3 hours. The reaction mixture was cooled to room temperature and allowed to stand overnight. The expected methyl 3-methyl-4-nitrobenzoate precipitated as light yellow crystals, which were collected by suction filtration yielding after drying 259.3 g. This solid was used as such in the next step.
후처리
- customIn a 5-liter three-necked round-bottomed flask equipped with a reflux condenser
- customwas bubbled in 20.8 g of hydrogen chloride
- temperaturethe resulting mixture was refluxed for 3 hours
- customThe expected methyl 3-methyl-4-nitrobenzoate precipitated as light yellow crystals, which
- filtrationwere collected by suction filtration
- customyielding
- customafter drying 259.3 g
출처 및 근거
- ORD 기록
- ord-732ac1daba234ece998973904b07adf1
- 출처 데이터셋
- uspto-grants-1999_07
- 특허 번호
- US05929098
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