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Water → 2-(2-Aminopurin-9-yl)methyl butan-1,4-diol

HRID 864987
ノート
印刷プレビュー

反応式

HRID 864987 の反応式
[NH2:1][C:2]1[N:10]=[C:9]2[C:5]([N:6]=[CH:7][N:8]2[CH2:11][CH:12]([CH2:17][C:18](OC)=[O:19])[C:13](OC)=[O:14])=[CH:4][N:3]=1.[BH4-].[Li+].O>C(O)(C)(C)C>[NH2:1][C:2]1[N:10]=[C:9]2[C:5]([N:6]=[CH:7][N:8]2[CH2:11][CH:12]([CH2:17][CH2:18][OH:19])[CH2:13][OH:14])=[CH:4][N:3]=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 4148881Lithium borohydrideHCID 19027589Dimethyl (2-aminopurin-9-ylmethyl)succinate

生成物 1

HCID 146200082-(2-Aminopurin-9-yl)methyl butan-1,4-diol

試薬・触媒・溶媒 1

HCID 6386tert-Butanol溶媒

実験手順

To a solution of crude dimethyl (2-aminopurin-9-ylmethyl)succinate (3.2 g, 10.9 mmol), dissolved in tert. butanol (250 ml) at 40° C., was added lithium borohydride (1.3 g, 60 mmol) in portions with stirring. After 1 hour at ambient temperature, water (30 ml) was added slowly and stirring continued over night. Inorganic salts were filtered and the solution evaporated to dryness. Yield of crude product was 1.6 g (50%). Chromatography on silica (chloroform+methanol 7+1) afforded pure product.

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. stirringstirring
  2. waitcontinued over night
  3. filtrationInorganic salts were filtered
  4. customthe solution evaporated to dryness
  5. customChromatography on silica (chloroform+methanol 7+1) afforded pure product

出典と根拠

ORDレコード
ord-225b8e07cc1d4468948ef84dd06751ba
出典データセット
uspto-grants-1996_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05565461

反応ノート

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