4-Fluoro-3-nitrobenzoic acid → 4-Fluoro-3-nitrobenzyl alcohol
반응식
[F:1][C:2]1[CH:10]=[CH:9][C:5]([C:6](O)=[O:7])=[CH:4][C:3]=1[N+:11]([O-:13])=[O:12].B.C1COCC1>C1COCC1>[F:1][C:2]1[CH:10]=[CH:9][C:5]([CH2:6][OH:7])=[CH:4][C:3]=1[N+:11]([O-:13])=[O:12]참가 물질
반응 조건
- 온도
- 0 °C
실험 절차
4-Fluoro-3-nitro-benzoic acid (185 mg, 1 mmol) was dissolved in THF (2 ml) and cooled to 0° C. under a nitrogen atmosphere. A Borane/THF solution (2 ml of a 1M solution, 2 mmol) was added dropwise, and the reaction mixture was heated to reflux for 1 h. The reaction was judged complete and quenched with 3N HCl (0.5 ml) and the solvent was removed under vacuum. The reaction mixture was partitioned between ethyl acetate and a sodium carbonate solution. The organic layer was washed with carbonate two additional times, and then it was washed with brine. It was dried over MgSO4, and the solvent was removed to yield the title product (160 mg (95%), 0.94 mmol). 1H NMR (DMSO-d6): δ=8.10 (s, 1H), 7.62 (d, J=7.3 Hz, 1H), 7.32 (d, J=7.3 Hz, 1H), 4.82 (d, J=4.5 Hz, 2H).
후처리
- temperaturethe reaction mixture was heated
- temperatureto reflux for 1 h
- customquenched with 3N HCl (0.5 ml)
- customthe solvent was removed under vacuum
- customThe reaction mixture was partitioned between ethyl acetate
- washThe organic layer was washed with carbonate two additional times
- washit was washed with brine
- dry with materialIt was dried over MgSO4
- customthe solvent was removed
출처 및 근거
- ORD 기록
- ord-e4b56798bafa4faa985207a78d440d2b
- 출처 데이터셋
- uspto-grants-2010_04
- 특허 번호
- US07696210B2
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