Sodium Hydroxide → 2-(2',3'-Dichloro[1,1'-biphenyl]-3-yl)propanedioic acid
반응식
C([O:3][C:4](=[O:25])[CH:5]([C:11]1[CH:12]=[C:13]([C:17]2[CH:22]=[CH:21][CH:20]=[C:19]([Cl:23])[C:18]=2[Cl:24])[CH:14]=[CH:15][CH:16]=1)[C:6]([O:8]CC)=[O:7])C.[OH-].[Na+]>>[Cl:24][C:18]1[C:19]([Cl:23])=[CH:20][CH:21]=[CH:22][C:17]=1[C:13]1[CH:14]=[CH:15][CH:16]=[C:11]([CH:5]([C:4]([OH:25])=[O:3])[C:6]([OH:8])=[O:7])[CH:12]=1참가 물질
3
반응 조건
- 온도
- 70 °C
실험 절차
2-(2′,3′-Dichloro-[1,1′-biphenyl]-3-yl)propanedioic acid 1,3-diethyl ester (i.e. the product of Step B, 0.30 g, 0.79 mmol) was added to 2% aqueous sodium hydroxide (5 mL), and the reaction mixture was heated at 70° C. for 20 min. The reaction mixture was cooled, quenched with 6 N aqueous hydrochloric acid, and extracted with ethyl acetate. The organic layer was separated, washed with brine, dried over sodium sulfate, and concentrated under reduced pressure to yield the title compound (0.20 g).
후처리
- temperatureThe reaction mixture was cooled
- customquenched with 6 N aqueous hydrochloric acid
- extractionextracted with ethyl acetate
- customThe organic layer was separated
- washwashed with brine
- dry with materialdried over sodium sulfate
- concentrationconcentrated under reduced pressure
출처 및 근거
- ORD 기록
- ord-01914ec508a6494a9a460b49abe1ee1a
- 출처 데이터셋
- uspto-grants-2014_05
- 특허 번호
- US08722690B2
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