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Ethylene Oxide → 5-(2-Hydroxyethyl)furan-2(3H)-one

HRID 2409381
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HRID 2409381 반응식
[O:1]1[CH:5]=[CH:4][CH:3]=[CH:2]1.[Li]CCCC.C[Si](Cl)(C)C.[CH2:16]1[O:18][CH2:17]1.C1C[O:22]CC1>>[OH:18][CH2:16][CH2:17][C:5]1[O:1][C:2](=[O:22])[CH2:3][CH:4]=1
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참가 물질

6

반응물 5

HCID 6354Ethylene OxideHCID 6397ChlorotrimethylsilaneHCID 8028TetrahydrofuranHCID 8029FuranHCID 178418339Butyllithium2회

생성물 1

HCID 116798165-(2-Hydroxyethyl)furan-2(3H)-one수율 54%

실험 절차

To a cooled solution of furan (3.40 g, 50.0 mmol) in THF (150 mL) was added n-BuLi (22 mL, 2.5M solution in hexane, 55.0 mmol) at 0° C. under inert gas atmosphere. The solution was allowed to warm to room temperature and stirred for 3 h. Then TMSCl (5.34 g, 50 mmol) was added dropwise at 0° C. and the solution was stirred for further 3 h at room temperature. Subsequently, the solution was again cooled to 0° C. and n-BuLi (22 mL, 2.5M solution in hexane, 55.0 mmol) was added a second time. After stirring for 3 h at room temperature ethyleneoxide (2.42 g, 55.0 mmol) was condensed by an acetone/dry ice condenser into the solution and the solution was stirred for further 12 h at room temperature. The mixture was quenched with aq NH4Cl, and then extracted with EtOAc and the combined organic layers were dried over Na2SO4 to afforded the desired product (5 g, 27.1 mmol, 54% over two steps) as a yellow liquid.

후처리

  1. stirringthe solution was stirred for further 3 h at room temperature
  2. temperatureSubsequently, the solution was again cooled to 0° C.
  3. customcondensed by an acetone/dry ice condenser into the solution
  4. stirringthe solution was stirred for further 12 h at room temperature
  5. customThe mixture was quenched with aq NH4Cl
  6. extractionextracted with EtOAc
  7. dry with materialthe combined organic layers were dried over Na2SO4

출처 및 근거

ORD 기록
ord-898d76b98ce24852b05e6954e9e98868
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08815873B2

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