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Diethyl Ether → (2R)-1-(benzyloxy)pent-4-en-2-ol

HRID 217984
Notes
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Reaction equation

HRID 217984 reaction equation
[CH3:1][CH2:2]OCC.[CH2:6]([O:10][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[C@@H:7]1[O:9][CH2:8]1.C([Mg]Cl)=C.[Cl-].[NH4+]>C1COCC1.[Cu]I>[CH2:11]([O:10][CH2:6][C@H:7]([OH:9])[CH2:8][CH:1]=[CH2:2])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 3283Diethyl EtherHCID 25517Ammonium ChlorideHCID 159746(-)-Benzyl (R)-glycidyl etherHCID 178461836HCID 178461836, compound

Product 1

HCID 10375318(2R)-1-(benzyloxy)pent-4-en-2-ol

Reagents, catalysts & solvents 2

HCID 24350
Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)
Catalyst
HCID 8028TetrahydrofuranSolvent

Conditions

Temperature
-78 °C

Procedure

Ether (100 ml) and copper(I) iodide (580 mg) were added to a solution of (R)-benzyl glycidyl ether (10.0 g) in THF (100 ml). The mixture was cooled to −78° C., and vinylmagnesium chloride (1.38 M, 53.0 ml) was added dropwise. The mixture was stirred overnight with gradual heating to room temperature. Ice was added to the reaction solution, and an ammonium chloride solution was further added. The aqueous layer was extracted with ethyl acetate, and the organic layer was washed with an ammonium chloride solution. The insoluble matter was removed by filtration through celite, and the solvent was evaporated under reduced pressure to obtain the title compound (12.5 g).

Workup

  1. temperaturewith gradual heating to room temperature
  2. additionIce was added to the reaction solution
  3. extractionThe aqueous layer was extracted with ethyl acetate
  4. washthe organic layer was washed with an ammonium chloride solution
  5. customThe insoluble matter was removed by filtration through celite
  6. customthe solvent was evaporated under reduced pressure

Sources & evidence

ORD record
ord-66d8431238374018b9428ed53cb30a46
Source dataset
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08198269B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes