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

HRID 1403681
ノート
印刷プレビュー

反応式

HRID 1403681 の反応式
[O:1]1[CH:5]=[CH:4][CH:3]=[CH:2]1.[Li]CCCC.[CH2:11]1[O:13][CH2:12]1.C1C[O:17]CC1>>[OH:13][CH2:11][CH2:12][C:5]1[O:1][C:2](=[O:17])[CH2:3][CH:4]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 4

HCID 6354Ethylene OxideHCID 8028TetrahydrofuranHCID 8029FuranHCID 178418339Butyllithium2 回

生成物 1

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

実験手順

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 TMSCI (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.

後処理

  1. additionThen TMSCI (5.34 g, 50 mmol) was added dropwise at 0° C.
  2. stirringthe solution was stirred for further 3 h at room temperature
  3. temperatureSubsequently, the solution was again cooled to 0° C.
  4. customcondensed by an acetone/dry ice condenser into the solution
  5. stirringthe solution was stirred for further 12 h at room temperature
  6. customThe mixture was quenched with aq NH4Cl
  7. extractionextracted with EtOAc
  8. dry with materialthe combined organic layers were dried over Na2SO4

出典と根拠

ORDレコード
ord-af8aa3f706c242d59559c4c91e5ff054
出典データセット
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08912209B2

反応ノート

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