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Nitric Acid → 4-Hydroxy-2,5-dimethyl-3-nitrobenzaldehyde

HRID 1271202
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HRID 1271202 반응식
[Cl-].[Na+].[OH:3][C:4]1[C:11]([CH3:12])=[CH:10][C:7]([CH:8]=[O:9])=[C:6]([CH3:13])[CH:5]=1.[N+:14]([O-])([OH:16])=[O:15]>S(=O)(=O)(O)O>[OH:3][C:4]1[C:11]([CH3:12])=[CH:10][C:7]([CH:8]=[O:9])=[C:6]([CH3:13])[C:5]=1[N+:14]([O-:16])=[O:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 944Nitric AcidHCID 5234Sodium ChlorideHCID 128272904-Hydroxy-2,5-dimethyl-benzaldehyde

생성물 1

HCID 184523704-Hydroxy-2,5-dimethyl-3-nitrobenzaldehyde

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매2회

실험 절차

To a −10° C. (ice and sodium chloride) solution of 4-hydroxy-2,5-dimethylbenzaldehyde (1.0 g, 6.65 mmol) in concentrated sulfuric acid (10 mL) was added dropwise 70% (concentrated) nitric acid (0.598 g, 6.65 mmol) in 2 mL concentrated sulfuric acid. The reaction stirred for approximately 30 minutes. The reaction was then poured onto crushed ice. The precipitate was collected and washed with water. The solid was then dried on a high vacuum pump to yield a white solid. Microanalysis (C9H9N1O4): calculated: C=55.39, H=4.65, N=7.18; found: C=55.60, H=4.65, N=7.02. MS: M+−1=194.1 Da.

후처리

  1. additionThe reaction was then poured
  2. customonto crushed ice
  3. customThe precipitate was collected
  4. washwashed with water
  5. customThe solid was then dried on a high vacuum pump
  6. customto yield a white solid

출처 및 근거

ORD 기록
ord-9b5335326da04d57887a62fa2e30869b
출처 데이터셋
uspto-grants-2007_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07205295B2

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