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 Bicarbonate → 1-[2-Hydroxy-5-(2-hydroxyethyl)phenyl]-ethanone

HRID 26672
ノート
印刷プレビュー

反応式

HRID 26672 の反応式
C([O:4][CH2:5][CH2:6][C:7]1[CH:12]=[CH:11][C:10]([OH:13])=[C:9]([C:14](=[O:16])[CH3:15])[CH:8]=1)(=O)C.C(=O)(O)[O-].[Na+]>C(O)C.O>[C:14]([C:9]1[CH:8]=[C:7]([CH:12]=[CH:11][C:10]=1[OH:13])[CH2:6][CH2:5][OH:4])(=[O:16])[CH3:15]
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 2

HCID 516892Sodium BicarbonateHCID 127698062-(3-Acetyl-4-hydroxyphenyl)ethyl acetate

生成物 1

HCID 127698071-[2-Hydroxy-5-(2-hydroxyethyl)phenyl]-ethanone収率 108.1%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 962Water溶媒

実験手順

A solution of 2-(3-acetyl-4-hydroxyphenyl)ethyl acetate (35.7 g) in ethanol (400 ml), and sodium bicarbonate (42 g) in water (200 mls) was refluxed for 81/2 hours. The ethanol was removed on a `Rotavapor` and the residue was extracted with ether (3x). The combined ethereal extracts were washed with water, sodium bicarbonate solution, saturated brine solution, dried over anhydrous magnesium sulphate, and evaporated to yield a red oil (31.3 g). The oil was recrystallised from hexane and ether (4:1) to yield the product as a pale yellow crystalline solid (18.3 g). The mother liquors were concentrated and an additional batch of product was obtained as a pale yellow crystalline solid (9.3 g).

後処理

  1. customThe ethanol was removed on a `Rotavapor` and the residue
  2. extractionwas extracted with ether (3x)
  3. washThe combined ethereal extracts were washed with water, sodium bicarbonate solution, saturated brine solution
  4. dry with materialdried over anhydrous magnesium sulphate
  5. customevaporated

出典と根拠

ORDレコード
ord-2d50ac568846435595ec3de54eebe546
出典データセット
uspto-grants-1979_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04151179

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