4-Methylmorpholine → HCID 178502897, 화합물
반응식
[SH:1][C:2]1[N:6]([CH2:7][C:8]([OH:10])=O)[N:5]=[N:4][N:3]=1.CN1CCOCC1.ClC(OCC)=O.Cl.[CH3:25][O:26][NH2:27]>O1CCCC1>[CH3:25][O:26][NH:27][C:8](=[O:10])[CH2:7][N:6]1[C:2]([SH:1])=[N:3][N:4]=[N:5]1참가 물질
실험 절차
To a solution cooled at -28° C. to -35° C. of 5-mercapto-1H-tetrazole-1-acetic acid (0.8 g) in tetrahydrofuran (40 ml) are added N-methylmorpholine (1.26 ml) and ethyl chloroformate (0.62 ml). After stirring for 1 hour, a solution of methoxyamine hydrochloride (0.34 g) and N-methylmorpholine (0.71 ml) in tetrahydrofuran (11 ml) is added to the mixture at -50° C. After 2 hours' stirring at about -30° C., the mixture is concentrated under reduced pressure, and the resultant mixture is diluted with water (50 ml) and ethyl acetate (50 ml). The mixture is acidified to pH 2 with hydrochloric acid and extracted with ethyl acetate. The extract solution is dried over magnesium sulfate and concentrated to give 5-mercapto-1H-tetrazole-1-acetohydroxamic acid methyl ester. mp. 165°-167° C. (decomp.).
후처리
- stirringAfter 2 hours' stirring at about -30° C.
- concentrationthe mixture is concentrated under reduced pressure
- additionthe resultant mixture is diluted with water (50 ml) and ethyl acetate (50 ml)
- extractionextracted with ethyl acetate
- dry with materialThe extract solution is dried over magnesium sulfate
- concentrationconcentrated
출처 및 근거
- ORD 기록
- ord-3a34622dbf2a435b8dd1bcae3112c30e
- 출처 데이터셋
- uspto-grants-1985_11
- 특허 번호
- US04555578
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