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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Nitric Acid → HCID 14366181, 화합물

HRID 1709610
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HRID 1709610 반응식
[CH2:1]([O:3][C:4]([NH:6][C:7]1[CH:12]=[CH:11][C:10]([NH:13][C:14]([O:16][CH2:17][CH3:18])=[O:15])=[CH:9][N:8]=1)=[O:5])[CH3:2].[N+:19]([O-])([OH:21])=[O:20]>S(=O)(=O)(O)O>[CH2:1]([O:3][C:4]([NH:6][C:7]1[CH:12]=[CH:11][C:10]([NH:13][C:14]([O:16][CH2:17][CH3:18])=[O:15])=[C:9]([N+:19]([O-:21])=[O:20])[N:8]=1)=[O:5])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 944Nitric AcidHCID 19878616HCID 19878616, 화합물

생성물 1

HCID 14366181HCID 14366181, 화합물

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

실험 절차

40 ml of concentrated sulphuric acid are cooled to 8° C. and 5 g of the compound of Stage 1 are added while stirring. At 5° C., 5 ml of concentrated nitric acid are then added dropwise and stirring is continued for 1 hour. Subsequently the mixture is poured on 300 to 400 g of ice and the precipitated crystals are isolated by filtering with suction 4 g of a yellow crystalline compound are obtained. On recrystallizing from ethanol this compound melts at 193° C. 1H-NMR Spectrum: 10.38 (s, NH), 9.72 (s, NH), 8.23 (d, J=9 Hz, 4-H), 8.10 (d, J=9 Hz, 3-H), 4.19d (q, J=7 Hz, OCH2), 4.13 (q, J=7 Hz, OCH2), 1.25 (t, J=7 Hz, CH3), 1.23 (t, J=7 Hz, CH3)

후처리

  1. stirringstirring
  2. customthe precipitated crystals are isolated
  3. filtrationby filtering with suction 4 g of a yellow crystalline compound
  4. customare obtained
  5. customOn recrystallizing from ethanol this compound melts at 193° C

출처 및 근거

ORD 기록
ord-4a3f53054bc54c248102e631c2ea7e07
출처 데이터셋
uspto-grants-1990_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04950302

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