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

HRID 1403681
Notes
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Reaction equation

HRID 1403681 reaction equation
[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
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 6354Ethylene OxideHCID 8028TetrahydrofuranHCID 8029FuranHCID 178418339Butyllithium2×

Product 1

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

Procedure

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.

Workup

  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

Sources & evidence

ORD record
ord-af8aa3f706c242d59559c4c91e5ff054
Source dataset
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08912209B2

Reaction notes

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