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Ethylene Oxide → 3-Butyn-1-ol, 4-(4-chlorophenyl)-

HRID 65226
Notes
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Reaction equation

HRID 65226 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]#[CH:9])=[CH:4][CH:3]=1.C([Li])CCC.[CH2:15]1[O:17][CH2:16]1.[Cl-].[NH4+]>C1COCC1>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]#[C:9][CH2:15][CH2:16][OH:17])=[CH:4][CH:3]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 6354Ethylene OxideHCID 25517Ammonium ChlorideHCID 70118Benzene, 1-chloro-4-ethynyl-HCID 178418339Butyllithium

Product 1

HCID 122603533-Butyn-1-ol, 4-(4-chlorophenyl)-

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Conditions

Temperature
-78 °C

Procedure

Dissolve 14.2 g (0.104 mole) of 1-chloro-4-ethynylbenzene in 35 ml dry THF and cool to -78° C. Add 49 ml butyl lithium to cold reaction mixture and allow to warm to room temperature for 2 hours. After 2 hours, cool to -78° C. and then add 5.8 ml (0.114 mole) ethylene oxide in 20 ml THF. Allow to warm to room temperature. Monitor progress of reaction with thin-layer chromatography on silica gel (methylene chloride). After 18 hours, add 150 ml saturated aqueous ammonium chloride solution and extract with 150 ml diethyl ether. Wash organic layer with 2×100 ml saturated aqueous sodium chloride solution. Dry organic layer with magnesium sulfate and then filter, and evaporate solvent to obtain the title compound.

Workup

  1. customto cold reaction mixture
  2. temperatureto warm to room temperature for 2 hours
  3. temperaturecool to -78° C.
  4. temperatureto warm to room temperature
  5. customMonitor progress of reaction with thin-layer chromatography on silica gel (methylene chloride)
  6. waitAfter 18 hours
  7. extractionextract with 150 ml diethyl ether
  8. filtrationDry organic layer with magnesium sulfate and then filter
  9. customevaporate solvent

Sources & evidence

ORD record
ord-01834e72521f43caa6f799cf0744450a
Source dataset
uspto-grants-1986_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04613609

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes