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Nitric Acid → 2-(2-Chloro-5-nitrophenyl)acetic acid

HRID 1517241
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HRID 1517241 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][C:9]([OH:11])=[O:10].[N+:12]([O-])([OH:14])=[O:13]>S(=O)(=O)(O)O>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N+:12]([O-:14])=[O:13])=[CH:4][C:3]=1[CH2:8][C:9]([OH:11])=[O:10]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 944Nitric AcidHCID 17124o-Chlorophenylacetic acid

생성물 1

HCID 8271282-(2-Chloro-5-nitrophenyl)acetic acid수율 80%

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매2회

반응 조건

온도
0 °C

실험 절차

A solution of 2-(2-chlorophenyl)acetic acid (500 mmol) in conc. sulfuric acid (0.7 mL/mmol) was cooled to −10° C. A freshly prepared mixture of fuming nitric acid fuming (809 mmol) and conc. sulfuric acid (1.6 mol) was slowly added at −10° C. The mixture was allowed to warm to 0° C. over 1 h and was stirred for 4 h at 0° C. The solution was slowly poured onto crushed ice/water (3 L). The mixture was stirred vigorously and the formed precipitate was isolated by filtration. The white solid residue was washed with an excess of water (4 L) and dried, giving 2-(2-chloro-5-nitrophenyl)acetic acid (80%).

후처리

  1. additionwas slowly added at −10° C
  2. additionThe solution was slowly poured
  3. stirringThe mixture was stirred vigorously
  4. customthe formed precipitate was isolated by filtration
  5. washThe white solid residue was washed with an excess of water (4 L)
  6. customdried

출처 및 근거

ORD 기록
ord-0a3464bbf7df4fa99ad029ed5f0f56e4
출처 데이터셋
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08232283B2

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