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Nitric Acid → HCID 86633440, 화합물

HRID 1881186
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HRID 1881186 반응식
[CH2:1]([O:3][C:4]1[C:5]([OH:15])=[CH:6][C:7]([N+:12]([O-:14])=[O:13])=[C:8]([CH:11]=1)[CH:9]=[O:10])[CH3:2].[N+:16]([O-])([OH:18])=[O:17]>ClCCl>[CH2:1]([O:3][C:4]1[C:5]([OH:15])=[C:6]([N+:16]([O-:18])=[O:17])[C:7]([N+:12]([O-:14])=[O:13])=[C:8]([CH:11]=1)[CH:9]=[O:10])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 944Nitric AcidHCID 450942415-Ethoxy-4-hydroxy-2-nitrobenzaldehyde

생성물 1

HCID 86633440HCID 86633440, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

5-Ethoxy-4-hydroxy-2-nitro-benzaldehyde (1.6 g) was dissolved in dichloromethane (30 ml) and a solution of nitric acid in dichloromethane (2M, 13 ml) was gradually added at a temperature under 30° C. The solution was stirred at room temperature for 10 min and then it was poured into ice-cold water. The organic phase was washed with water and then it was dried and evaporated.

후처리

  1. additionit was poured into ice-cold water
  2. washThe organic phase was washed with water
  3. customit was dried
  4. customevaporated

출처 및 근거

ORD 기록
ord-54c530f1a88d424cae06118e9b210021
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08318785B2

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