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

Sodium Hydroxide → HCID 59606751、化合物

HRID 1627927
ノート
印刷プレビュー

反応式

HRID 1627927 の反応式
C(N(CC)C(=O)[O:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([Cl:12])[C:7]=1[CH2:13][CH2:14][CH2:15][OH:16])C.[OH-].[Na+]>C(O)C>[Cl:12][C:8]1[C:7]([CH2:13][CH2:14][CH2:15][OH:16])=[C:6]([OH:5])[CH:11]=[CH:10][CH:9]=1
参加物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 14798Sodium HydroxideHCID 59606761HCID 59606761、化合物

生成物 1

HCID 59606751HCID 59606751、化合物収率 213.6%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To a solution of the 3-chloro-2-(3-hydroxypropyl)phenyl diethylcarbamate (0.410 g; 1.43 mmol) in ethanol (14.5 ml) was added solid sodium hydroxide (0.144 g; 3.59 mmol) and the reaction mixture was heated at reflux for 21 h. After cooling, the volatiles were removed under reduced pressure, water was added and the mixture was extracted with diethyl ether, the combined organics were dried over magnesium sulphate, filtered and concentrated under reduced pressure. Purification by flash chromatography on silica gel using a gradient of ethyl acetate (15-100%) in heptane furnished 0.57 g (79%) of the desired 3-chloro-2-(3-hydroxypropyl)phenol.

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

後処理

  1. temperaturethe reaction mixture was heated
  2. temperatureat reflux for 21 h
  3. temperatureAfter cooling
  4. customthe volatiles were removed under reduced pressure, water
  5. additionwas added
  6. extractionthe mixture was extracted with diethyl ether
  7. dry with materialthe combined organics were dried over magnesium sulphate
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure
  10. customPurification by flash chromatography on silica gel using a gradient of ethyl acetate (15-100%) in heptane

出典と根拠

ORDレコード
ord-f77bb94f068d4459bb906d426aed348c
出典データセット
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08785638B2

反応ノート

読み込み中…