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

Water → 2-(3,5-Dichlorophenyl)acetic acid

HRID 322637
ノート
印刷プレビュー

反応式

HRID 322637 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([CH2:9][C:10]#N)[CH:5]=[C:6]([Cl:8])[CH:7]=1.S(=O)(=O)(O)[OH:13].[OH2:17]>CCCCCC>[Cl:1][C:2]1[CH:3]=[C:4]([CH2:9][C:10]([OH:13])=[O:17])[CH:5]=[C:6]([Cl:8])[CH:7]=1
参加物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 AcidHCID 126899782-(3,5-Dichlorophenyl)acetonitrile

生成物 1

HCID 64524872-(3,5-Dichlorophenyl)acetic acid

試薬・触媒・溶媒 1

HCID 8058Hexane溶媒

実験手順

The nitrile was added to a mixture of 40 mL of concentrated sulfuric acid and 50 mL H2O and heated to reflux for 48 hours, cooled to room temperature and stirred for 48 hours. The reaction was diluted into 1 L of crushed ice, warmed to room temperature and extracted with 2×200 mL of dichloromethane and 2×200 mL of ethylacetate. Both sets of organics were combined and washed with saturated aqueous NaHCO3. The NaHCO3 fractions were combined and acidified to pH 1 with 3N HCl. The white solid was too fine to filter and was extracted out with 2×200 mL of dichloromethane. The combined organics were dried with Na2SO4 and the solvents removed at reduced pressure to yield crude 3,5-dichlorophenylacetic acid as a white solid. The solid was slurried with hexane and filtered to get 1.75 g of white solid.

後処理

  1. temperatureheated
  2. temperatureto reflux for 48 hours
  3. temperaturewarmed to room temperature
  4. extractionextracted with 2×200 mL of dichloromethane and 2×200 mL of ethylacetate
  5. washwashed with saturated aqueous NaHCO3
  6. filtrationto filter
  7. extractionwas extracted out with 2×200 mL of dichloromethane
  8. dry with materialThe combined organics were dried with Na2SO4
  9. customthe solvents removed at reduced pressure
  10. customto yield crude 3,5-dichlorophenylacetic acid as a white solid
  11. filtrationfiltered

出典と根拠

ORDレコード
ord-32fe12fee72c4a938265988a1ba6f1b5
出典データセット
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06211235B1

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート