ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

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

HRID 1517241
ノート
印刷プレビュー

反応式

HRID 1517241 の反応式
[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]
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

4

反応物 2

HCID 944Nitric AcidHCID 17124o-Chlorophenylacetic acid

生成物 1

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

試薬・触媒・溶媒 1

HCID 1118Sulfuric Acid溶媒2 回

反応条件

温度
0 °C

実験手順

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%).

後処理

  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

出典と根拠

ORDレコード
ord-0a3464bbf7df4fa99ad029ed5f0f56e4
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

読み込み中…

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