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Tetrahydrofuran → Fur-2-ylmethyl 2-hydroxyethyl ether

HRID 582065
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HRID 582065 반응식
[O:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH2:6][O:7][CH2:8][C:9](OCC)=[O:10].O1CCCC1.[H-].[Al+3].[Li+].[H-].[H-].[H-].[OH-].[Na+]>C(OCC)(=O)C.ClCCl.O>[OH:10][CH2:9][CH2:8][O:7][CH2:6][C:2]1[O:1][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 8028TetrahydrofuranHCID 14798Sodium HydroxideHCID 14746268Ethyl fur-2-ylmethoxyacetateHCID 21226445Aluminium lithium hydride

생성물 1

HCID 10103270Fur-2-ylmethyl 2-hydroxyethyl ether

시약·촉매·용매 2

HCID 962Water용매2회
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
HCID 21226138
Dichloromethane ethylacetate
용매

실험 절차

Combine ethyl 2-fur-2-ylmethoxyaceate (1.2 g, 6.5 mmol) and tetrahydrofuran (10 mL). Cool in an ice-bath. Add dropwise a solution of lithium aluminum hydride (8.0 mL, 1.0M in THF, 8.0 mmol). After 2 hours, add water (0.3 mL), add 15% sodium hydroxide solution (0.3 mL), and add water (0.9 mL). Stir vigorously. After 15 minutes, filter the reaction mixture and dry the filtrate over Na2SO4, filter, and concentrate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with 2% ethyl acetate/dichloromethane to give fur-2-ylmethyl 2-hydroxyethyl ether: Rf =0.22 (silica gel, 5% acetone/dichloromethane).

후처리

  1. temperatureCool in an ice-bath
  2. waitAfter 15 minutes
  3. filtrationfilter the reaction mixture
  4. dry with materialdry the filtrate over Na2SO4
  5. filtrationfilter
  6. concentrationconcentrate in vacuo
  7. customto give a residue

출처 및 근거

ORD 기록
ord-9cb62d9ba8a04fcd9d19f9861564f69d
출처 데이터셋
uspto-grants-1999_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05922737

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