반응식
[F:1][C:2]1[CH:3]=[C:4]([CH:19]=[CH:20][CH:21]=1)[CH2:5][O:6][C:7]1[CH:15]=[CH:14][C:10]([C:11]([OH:13])=O)=[C:9]([N+:16]([O-])=O)[CH:8]=1.FC1C=C(C=CC=1)COC(=O)[C:29]1C=CC(OCC2C=CC=C(F)C=2)=C[C:30]=1[N+:44]([O-])=O.COC(=O)C1C=CC(OCC2C=CC=C(F)C=2)=CC=1[N+:69]([O-])=O.O.[OH-].[Li+].[OH-].[Na+].[CH2:78]1[CH2:82][O:81]CC1>O>[F:1][C:2]1[CH:3]=[C:4]([CH:19]=[CH:20][CH:21]=1)[CH2:5][O:6][C:7]1[CH:8]=[C:9]2[C:10]([C:11](=[O:13])[N:44]([CH2:78][C:82]([NH2:69])=[O:81])[C:30]([CH3:29])=[N:16]2)=[CH:14][CH:15]=1참가 물질
반응물 6
생성물 1
시약·촉매·용매 1
실험 절차
4-(3-Fluoro-benzyloxy)-2-nitro-benzoic acid: A mixture of 4-(3-fluorobenzyloxy)-2-nitro-benzoic acid (3-fluoro-benzyl) ester and 4-(3-fluoro-benzyloxy)-2-nitro-benzoic acid methyl ester (14.0 g, 35.0 mmol) in THF (120 mL) and water (120 mL), containing lithium hydroxide monohydrate (2.94 g, 70.1 mmol) was stirred at rt for 48 h. Then the mixture was poured into sodium hydroxide (2 N, 50 mL) and then the mixture extracted with diethyl ether (3×150 mL). The aqueous phase was then adjusted to pH 2 with HCl. Then the mixture was poured into sodium hydroxide (2 N, 50 mL) and the aqueous phase was then adjusted to pH 5.2 with HCl then the mixture extracted with diethyl ether (3×100 mL). The combined extracts were then washed with brine (100 mL) dried and evaporated to afford title compound (6.6 g, 65%) as a light yellow solid. MS: m/e=290.0 (M−H).
후처리
- extractionthe mixture extracted with diethyl ether (3×150 mL)
- additionThen the mixture was poured into sodium hydroxide (2 N, 50 mL)
- extractionthe mixture extracted with diethyl ether (3×100 mL)
- washThe combined extracts were then washed with brine (100 mL)
- customdried
- customevaporated
출처 및 근거
- ORD 기록
- ord-ad3689421b0444ecba177dceb56a6917
- 출처 데이터셋
- uspto-grants-2006_08
- 특허 번호
- US07087612B2
연결된 노트
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