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Potassium Nitrate → HCID 67024029, 화합물

HRID 450738
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HRID 450738 반응식
[CH2:1]([N:4]1[CH2:16][CH2:15][C:14]2[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[N:7]([C:17](=[O:19])[CH3:18])[C:6]=2[CH2:5]1)[CH2:2][CH3:3].[N+:20]([O-])([O-:22])=[O:21].[K+]>OS(O)(=O)=O>[N+:20]([C:10]1[CH:9]=[C:8]2[C:13]([C:14]3[CH2:15][CH2:16][N:4]([CH2:1][CH2:2][CH3:3])[CH2:5][C:6]=3[N:7]2[C:17](=[O:19])[CH3:18])=[CH:12][CH:11]=1)([O-:22])=[O:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24434Potassium NitrateHCID 67023909HCID 67023909, 화합물

생성물 1

HCID 67024029HCID 67024029, 화합물수율 97.1%

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

실험 절차

To 1-(2-propyl-1,2,3,4-tetrahydro-beta-carbolin-9-yl)-ethanone (1.05 g, 4.1 mmol) in conc. H2SO4 was added KNO3 (435 mg, 4.3 mmol) in small portions at 0° C. The reaction mixture was allowed to warm up to room temperature and stirred for an additional 30 minutes. The reaction mixture was poured onto 250 ml of ice and extracted once with ethyl acetate. The aqueous phase was made alkaline and extracted twice with ethyl acetate. The combined organic phases were dried over magnesium sulfate, filtered, and evaporated to dryness to yield 1.2 g of crude product (70% purity).

후처리

  1. extractionextracted once with ethyl acetate
  2. extractionextracted twice with ethyl acetate
  3. dry with materialThe combined organic phases were dried over magnesium sulfate
  4. filtrationfiltered
  5. customevaporated to dryness

출처 및 근거

ORD 기록
ord-8e88bde265c9498298c2fe59eaf4fc9e
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08486984B2

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