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1,4-Butanediol → 4-Nonyloxybutanol

HRID 439748
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인쇄 미리보기

반응식

HRID 439748 반응식
[CH2:1]([OH:6])[CH2:2][CH2:3][CH2:4][OH:5].[H-].[Na+].Br[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18]>CN(C)C=O>[CH2:10]([O:5][CH2:4][CH2:3][CH2:2][CH2:1][OH:6])[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 80641,4-ButanediolHCID 127421-BromononaneHCID 24758Sodium hydride

생성물 1

HCID 224079404-Nonyloxybutanol

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a solution of 7.1 ml of 1,4-butanediol in 40 ml of dimethylformamide, 1.8 gms of sodium hydride are added; and the reaction mixture is stirred at room temperature for 15 minutes. To this solution is added 7.6 ml of bromononane and the reaction mixture is stirred at room temperature for 44 hours. The reaction mixture is then partitioned between ethyl acetate and water and the organic layer is washed with brine, dried over sodum sulfate, filtered, and concentrated under vacuum. The residue is flash chromatographed with an 8/1 ratio of ethyl acetate and hexane to give 4-nonyloxybutanol as a clear colorless liquid.

후처리

  1. stirringthe reaction mixture is stirred at room temperature for 44 hours
  2. customThe reaction mixture is then partitioned between ethyl acetate and water
  3. washthe organic layer is washed with brine
  4. dry with materialdried over sodum sulfate
  5. filtrationfiltered
  6. concentrationconcentrated under vacuum
  7. customchromatographed with an 8/1 ratio of ethyl acetate and hexane

출처 및 근거

ORD 기록
ord-dcffb15bac664b1680da6a2bfc1e2717
출처 데이터셋
uspto-grants-1996_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05516767

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