Acetone → HCID 54557443, 화합물
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[C:1](=[S:6])([S-:5])[S:2][CH2:3][CH3:4].[K+].C(O[CH:12]1[NH:15][C:14](=[O:16])[CH:13]1[CH:17]([CH3:19])[CH3:18])(=O)C.CC(C)=O.C1(C)C=CC=CC=1.C(OCC)(=O)C>O>[CH2:3]([S:2][C:1]([S:5][CH:12]1[NH:15][C:14](=[O:16])[CH:13]1[CH:17]([CH3:19])[CH3:18])=[S:6])[CH3:4]참가 물질
실험 절차
A solution of 230 mg of potassium ethyl trithiocarbonate in 1.5 ml of water is added dropwise at room temperature, in a nitrogen atmosphere, to a solution of 195 mg (1.14 mmole) of 4-acetoxy-3-isopropylazetidin-2-one (racemic mixture of cis- and trans-isomer in the ratio of 1:3) in 1 ml of water and 0.2 ml of acetone and the mixture is stirred at the same temperature for 120 minutes. The reaction mixture is exhaustively extracted with methylene chloride. The combined organic phases are dried over sodium sulphate and concentrated by evaporation in vacuo. The residue is chromatographed over 12 g of silica gel with toluene/ethyl acetate (9:1) and yields the trans-title compound. Melting point: 65°-66° TLC: Rf =0.5 (toluene/ethyl acetate 2:3]; IR spectrum (CH2Cl2): absorption bands at 2.95, 3.37, 5.62 and 9.25μ. NMR spectrum (in CDCl3 /100 Mc, in ppm): 6.65, 1H, m (exchange with D2O); 5.4, 1 H, d (J=2.5 Hz): 3.39, 2H, q; 3.05, 1H, m; 2.15, 1H, m: 1.38, 3H, t; 1.1, 6H, m.
후처리
- extractionThe reaction mixture is exhaustively extracted with methylene chloride
- dry with materialThe combined organic phases are dried over sodium sulphate
- concentrationconcentrated by evaporation in vacuo
- customThe residue is chromatographed over 12 g of silica gel with toluene/ethyl acetate (9:1)
- customyields the trans-title compound
- customIR spectrum (CH2Cl2): absorption bands at 2.95, 3.37, 5.62 and 9.25μ
출처 및 근거
- ORD 기록
- ord-7c04ecce676245b5971aab88bdebed49
- 출처 데이터셋
- uspto-grants-1990_08
- 특허 번호
- US04952690
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