Nitric Acid → Isosorbide Mononitrate

HRID 1735679노트

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HRID 1735679 반응식
CC([O:4][C@@H:5]1[C@H:9]2[O:10][CH2:11][C@@H:12]([OH:13])[C@H:8]2[O:7][CH2:6]1)=O.[N+:14]([O-])([OH:16])=[O:15].C(=O)([O-])[O-].[K+].[K+]>C(O)(=O)C.C(OC(=O)C)(=O)C.CO>[CH2:11]1[O:10][C@@H:9]2[C@H:5]([O:4][N+:14]([O-:16])=[O:15])[CH2:6][O:7][C@@H:8]2[C@H:12]1[OH:13]

참가 물질

7

실험 절차

For this isosorbide-2-acetate is for example firstly nitrated with nitric acid in glacial acetic acid or acetic acid anhydride and subsequently the acetate group is cleaved off with potassium carbonate in methanol. In this process isosorbide-5-nitrate is obtained in an isomerically pure form and in excellent yield (FIG. 1).

출처 및 근거

ORD 기록
ord-5c0e6cbd81b24705889798c2a33ccf82
출처 데이터셋
uspto-grants-1996_07
특허 번호
US05538891

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