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Tetrahydrofuran → 1-(3-Hydroxypropyl)-1,2,3-triazole

HRID 2222420
ノート
印刷プレビュー

反応式

HRID 2222420 の反応式
[N:1]1([CH:6]([CH3:12])C(OCC)=O)[CH:5]=[CH:4][N:3]=[N:2]1.[H-].[Al+3].[Li+].[H-].[H-].[H-].[OH-].[Na+].C1C[O:24][CH2:23]C1>>[N:1]1([CH2:6][CH2:12][CH2:23][OH:24])[CH:5]=[CH:4][N:3]=[N:2]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

5

反応物 4

HCID 8028Tetrahydrofuran2 回HCID 14798Sodium HydroxideHCID 14196987ethyl (1H-1,2,3-triazol-1-yl)propanoateHCID 21226445Aluminium lithium hydride

生成物 1

HCID 220309141-(3-Hydroxypropyl)-1,2,3-triazole収率 92%

反応条件

温度
0 °C

実験手順

A solution of ethyl (1H-1,2,3-triazol-1-yl)propanoate (8.96 g, 53 mmol) in THF (50 ml) was added dropwise to a suspension of lithium aluminium hydride (3 g, 79 mmol) in THF (250 ml) cooled at 0° C. After stirring for 1 hour at 5° C., the mixture was stirred for 1 hour at ambient temperature. The mixture was cooled at 0° C. and 4N sodium hydroxide (30 ml) was added dropwise. The mixture was filtered and the solid was washed with THF followed by ethyl acetate. The filtrate was dried (MgSO4) and evaporated. The residue was purified by column chromatography, eluting with methylene chloride/methanol (94/6) to give 3-(1,2,3-triazol-1-yl)propan-1-ol (6.2 g, 92%).

後処理

  1. stirringthe mixture was stirred for 1 hour at ambient temperature
  2. temperatureThe mixture was cooled at 0° C.
  3. filtrationThe mixture was filtered
  4. washthe solid was washed with THF
  5. dry with materialThe filtrate was dried (MgSO4)
  6. customevaporated
  7. customThe residue was purified by column chromatography
  8. washeluting with methylene chloride/methanol (94/6)

出典と根拠

ORDレコード
ord-a014692a349a46cfbd78321a17734438
出典データセット
uspto-grants-2008_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07371765B2

反応ノート

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