Phosphate → 3-Phenylacetamido-4-(2-hydroxyethyl)-2-azetidinone
반응식
O1CCCCC1[N:7]1[CH:10]([CH2:11][CH2:12][O:13]C2CCCCO2)[CH:9]([NH:20][C:21](=[O:29])[CH2:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[C:8]1=[O:30].O.C1(C)C=CC(S(O)(=O)=O)=CC=1.P([O-])([O-])([O-])=O>CO>[C:23]1([CH2:22][C:21]([NH:20][CH:9]2[CH:10]([CH2:11][CH2:12][OH:13])[NH:7][C:8]2=[O:30])=[O:29])[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1참가 물질
5
실험 절차
A solution of 1-(2-tetrahydropyranyl)-3-phenylacetamido-4-[2-(2-tetrahydropyranyl)oxyethyl]-2-azetidinone in methanol at 25° C. is treated with 0.1 molar equivalent of p-toluenesulfonic acid monohydrate. The solution is stirred for a period of 2 hours and then neutralized with 1 M pH 7 phosphate buffer. The product is extracted into ethyl acetate. The ethyl acetate solution is washed with brine, dried over magnesium sulfate and filtered. The filtrate is evaporated under reduced pressure to give 3-phenylacetamido-4-(2-hydroxyethyl)-2-azetidinone.
후처리
- extractionThe product is extracted into ethyl acetate
- washThe ethyl acetate solution is washed with brine
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- customThe filtrate is evaporated under reduced pressure
출처 및 근거
- ORD 기록
- ord-6da8ac6050c642649f28e4ed0a82a149
- 출처 데이터셋
- uspto-grants-1980_08
- 특허 번호
- US04218463
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