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

HRID 1517249
ノート
印刷プレビュー

反応式

HRID 1517249 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 1118Sulfuric Acid2 回HCID 11414995Dimethyl 2-(2-chloro-4-nitrophenyl)malonate

生成物 1

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

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

反応条件

温度
80 °C

実験手順

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

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%).

後処理

  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

出典と根拠

ORDレコード
ord-ef6da61c70e44ad6b42210fe8b0c91e7
出典データセット
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08232283B2

反応ノート

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