반응식
BrC1C=CC(C(O)=O)=CC=1.C([Li])CCC.O1CC(=O)C1.Cl.[OH:22][C:23]1([C:27]2[CH:35]=[CH:34][C:30]([C:31]([OH:33])=[O:32])=[CH:29][CH:28]=2)[CH2:26][O:25][CH2:24]1.C(O)(=O)C1C=CC=CC=1>C1COCC1.C(OCC)(=O)C>[OH:22][C:23]1([C:27]2[CH:28]=[CH:29][C:30]([C:31]([OH:33])=[O:32])=[CH:34][CH:35]=2)[CH2:26][O:25][CH2:24]1참가 물질
실험 절차
To 4-bromobenzoic acid (434 mg, 2.16 mmol) in THF (9 mL) at −78° C. was added dropwise n-butyllithium (2.84 mL of 1.6 M in hexanes, 4.54 mmol). The reaction mixture was stirred for 30 minutes, then oxetan-3-one (218 mg, 3.03 mmol) in THF (1 mL) was added dropwise. The reaction mixture was stirred for 30 minutes at −78° C. and allowed to warm to room temperature over 30 minutes. The reaction mixture was diluted with ethyl acetate (15 mL) and acidified to pH 2 with 2 N HCl. The layers were separated and the aqueous was re-extracted with ethyl acetate (15 mL). The combined organics were washed with brine solution (10 mL), dried over MgSO4 and concentrated in vacuo to give a white solid as a 1:1 mixture of 4-(3-hydroxyoxetan-3-yl)benzoic acid/benzoic acid (380 mg, 91%).
후처리
- stirringThe reaction mixture was stirred for 30 minutes at −78° C.
- customThe layers were separated
- extractionthe aqueous was re-extracted with ethyl acetate (15 mL)
- washThe combined organics were washed with brine solution (10 mL)
- dry with materialdried over MgSO4
- concentrationconcentrated in vacuo
- customto give a white solid
출처 및 근거
- ORD 기록
- ord-4cd6ef90f71d4dc68992b3443b607049
- 출처 데이터셋
- uspto-grants-2014_09
- 특허 번호
- US08828996B2
연결된 노트
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