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1-Butanol → 1-Butoxy-3-(phenylmethoxy)propan-2-ol

HRID 1382497
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인쇄 미리보기

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HRID 1382497 반응식
[CH2:1]([OH:5])[CH2:2][CH2:3][CH3:4].[H-].[Na+].[CH2:8]([O:15][CH2:16][CH:17]1[O:19][CH2:18]1)[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1>CN(C=O)C.O>[CH2:1]([O:5][CH2:18][CH:17]([OH:19])[CH2:16][O:15][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[CH2:2][CH2:3][CH3:4]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 2631-ButanolHCID 24758Sodium hydride2회HCID 94247Benzyl glycidyl ether

생성물 1

HCID 30211351-Butoxy-3-(phenylmethoxy)propan-2-ol수율 48.2%

시약·촉매·용매 2

HCID 962Water용매HCID 6228Dimethylformamide용매2회

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온도
80 °C

실험 절차

n-Butanol (2.5 ml, 27 mmol) is added to a suspension of sodium hydride (50% in mineral oil; 1.3 g, 27 mmol) in DMF (5 ml) and the mixture is then heated to 80° C. for 1.0 hours when all the sodium hydride is consumed. A solution of 2,3-epoxypropyl benzyl ether (benzyl glycidylether*) (4.52 g, 27 mmol) in DMF (5 ml) is added slowly to the n-butoxide solution. The mixture is then heated to 80° C. for 16 hours, diluted with water and extracted with ether. The ether layer is dried and concentrated to give an oil which is distilled to provide the desired product (3.1 g), bp 125°-130°/0.8-0.5 mm.

후처리

  1. customis consumed
  2. extractionextracted with ether
  3. dry with materialThe ether layer is dried
  4. concentrationconcentrated
  5. customto give an oil which
  6. distillationis distilled

출처 및 근거

ORD 기록
ord-82dc045f818645d999e6df1ac0c7379a
출처 데이터셋
uspto-grants-1989_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04806642

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