반응식
C([O:4][C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([O:11][CH2:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH:6]=1)(=O)C.[OH-].[Na+].Cl>O1CCCC1>[CH2:12]([O:11][C:7]1[CH:6]=[C:5]([OH:4])[CH:10]=[CH:9][CH:8]=1)[C:13]1[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1참가 물질
5
실험 절차
3-Benzyloxyphenyl acetate (4.84 g, 20 mmol), as prepared in the preceding step, in tetrahydrofuran (50 mL) was treated with 1 N NaOH (30 mL) at room temperature for 3 h. The mixture was acidified with 1 N HCl and extracted with ethyl acetate (3×100 mL). The organic phase was washed with brine (2×50 mL) and dried over Na2SO4. The solvent was removed in vacuo and the residue purified by flash column chromatography (methylene chloride) to give the title compound as a colorless liquid (3.80 g, 96%).
후처리
- extractionextracted with ethyl acetate (3×100 mL)
- washThe organic phase was washed with brine (2×50 mL)
- dry with materialdried over Na2SO4
- customThe solvent was removed in vacuo
- customthe residue purified by flash column chromatography (methylene chloride)
출처 및 근거
- ORD 기록
- ord-4630dc38332540efb92661ade97ed0bd
- 출처 데이터셋
- uspto-grants-2001_08
- 특허 번호
- US06281206B1
연결된 노트
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