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Sodium Hydroxide → O-methoxymethyl-N-methyl-N-(2-nitrophenylthio)-beta-hydroxytyrosine

HRID 1587284
ノート
印刷プレビュー

反応式

HRID 1587284 の反応式
[CH3:1][O:2][CH2:3][O:4][C:5]1[CH:18]=[CH:17][C:8]([CH:9]([OH:16])[C@@H:10]([C:13]([OH:15])=[O:14])[NH:11][CH3:12])=[CH:7][CH:6]=1.C[Si](C([Si](C)(C)C)C(N)=O)(C)C.[N+:31]([C:34]1[CH:39]=[CH:38][CH:37]=[CH:36][C:35]=1[S:40]Cl)([O-:33])=[O:32].[OH-].[Na+]>ClCCl>[CH3:1][O:2][CH2:3][O:4][C:5]1[CH:6]=[CH:7][C:8]([CH:9]([OH:16])[C@@H:10]([C:13]([OH:15])=[O:14])[N:11]([CH3:12])[S:40][C:35]2[CH:36]=[CH:37][CH:38]=[CH:39][C:34]=2[N+:31]([O-:33])=[O:32])=[CH:17][CH:18]=1
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

6

反応物 4

HCID 14798Sodium HydroxideHCID 243192-Nitrobenzenesulfenyl chloride2 回HCID 11708267Bistrimethylsilylacetamid2 回HCID 53901170O-methoxymethyl-N-methyl-beta-hydroxytyrosine

生成物 1

HCID 54196694O-methoxymethyl-N-methyl-N-(2-nitrophenylthio)-beta-hydroxytyrosine収率 85%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

反応条件

温度
0 °C

実験手順

To a solution of O-methoxymethyl-N-methyl-β-hydroxytyrosine (15.1 g) and bis(trimethylsilyl)acetamide (25 ml) in dichloromethane (150 ml) was added a solution of 2-nitrophenylsulfenyl chloride (11.2 g) in dichloromethane (50 ml). After stirring for 2 hours at 0° C., bis(trimethylsilyl)acetamide (10 ml) and 2-nitrophenylsulfenyl chloride (5.6 g) was added to the solution. The mixture was stirred for 3 hours at room temperature and added to 1N-sodium hydroxide (200 ml). The organic layer was washed with water (300 ml) and the aqueous solutions were combined. After the aqueous solution was acidified with diluted hydrochloric acid, the product was extracted with ethyl acetate (300 ml) and the extract was washed with water (100 ml×3). After the solution was dried over magnesium sulfate, the solvent was removed in vacuo to give O-methoxymethyl-N-methyl-N-(2-nitrophenylthio)-β-hydroxytyrosine (20.5 g).

後処理

  1. stirringThe mixture was stirred for 3 hours at room temperature
  2. washThe organic layer was washed with water (300 ml)
  3. extractionthe product was extracted with ethyl acetate (300 ml)
  4. washthe extract was washed with water (100 ml×3)
  5. dry with materialAfter the solution was dried over magnesium sulfate
  6. customthe solvent was removed in vacuo

出典と根拠

ORDレコード
ord-51a3820cfad94e8ba290507c4c7ed349
出典データセット
uspto-grants-1993_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05217952

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