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

HRID 1791730
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HRID 1791730 반응식
[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
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참가 물질

5

반응물 4

HCID 8028Tetrahydrofuran2회HCID 14798Sodium HydroxideHCID 14196987ethyl (1H-1,2,3-triazol-1-yl)propanoateHCID 21226445Aluminium lithium hydride

생성물 1

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

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온도
0 °C

실험 절차

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%).

후처리

  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)

출처 및 근거

ORD 기록
ord-b9bcb2b3e3484d9183f9971b312dfb5b
출처 데이터셋
uspto-grants-2006_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07074800B1

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