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Water → 2-(2-Chloro-4-nitrophenyl)acetic acid

HRID 1517249
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반응식

HRID 1517249 반응식
[Cl:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[CH:11](C(OC)=O)[C:12]([O:14]C)=[O:13].S(=O)(=O)(O)O.O>C(O)(=O)C>[Cl:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[CH2:11][C:12]([OH:14])=[O:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 1118Sulfuric Acid2회HCID 11414995Dimethyl 2-(2-chloro-4-nitrophenyl)malonate

생성물 1

HCID 125105882-(2-Chloro-4-nitrophenyl)acetic acid수율 80%

시약·촉매·용매 1

HCID 176Acetic Acid용매

반응 조건

온도
80 °C
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실험 절차

Dimethyl 2-(2-chloro-4-nitrophenyl)malonate (96 mmol) was suspended in acetic acid (175 mL). Conc. sulfuric acid (3.5 mL) was added and the mixture was stirred at 80° C. over night. Water (30 mL) was added and the mixture was stirred at 100° C. for 2 h. after which conc. sulfuric acid (1 mL) was added. The mixture was stirred at room temperature over night. The formed precipitate was filtered off and washed with water. The remaining solid was dried under reduced pressure to give 2-(2-chloro-4-nitrophenyl)acetic acid as a solid (80%).

후처리

  1. additionwas added
  2. stirringThe mixture was stirred at room temperature over night
  3. filtrationThe formed precipitate was filtered off
  4. washwashed with water
  5. customThe remaining solid was dried under reduced pressure

출처 및 근거

ORD 기록
ord-ef6da61c70e44ad6b42210fe8b0c91e7
출처 데이터셋
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08232283B2

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