(1,1'-Biphenyl)-3-ol, 4-nitro- → 2-Amino-5-phenylphenol
반응식
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:6][C:5]=1[OH:16])([O-])=O>C(O)C.[Pd]>[NH2:1][C:4]1[CH:9]=[CH:8][C:7]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:6][C:5]=1[OH:16]참가 물질
4
실험 절차
8.8 g (40 mmol) of 4-nitro-1,1′-biphenyl-3-ol from step B was dissolved in 120 mL of ethanol and hydrogenated in the presence of 0.8 g of a palladium-activated carbon catalyst (10%) at 25° C. After the required quantity of hydrogen had been absorbed, the catalyst was filtered off, and the solvent was distilled off in a rotary evaporator. This gave 7.3 g of 4° amino-1,1′-biphenyl-3-ol.
후처리
- customAfter the required quantity of hydrogen had been absorbed
- filtrationthe catalyst was filtered off
- distillationthe solvent was distilled off in a rotary evaporator
- customThis gave 7.3 g of 4° amino-1,1′-biphenyl-3-ol
출처 및 근거
- ORD 기록
- ord-6df45d51665c49f09d124502c444021a
- 출처 데이터셋
- uspto-grants-2006_10
- 특허 번호
- US07122061B2
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