3393-45-1 → 2H-Pyran-2-one, 4-ethenyltetrahydro-
Reaction equation
[CH:1]([Li])=[CH2:2].[O:4]1[CH2:9][CH2:8][CH:7]=[CH:6][C:5]1=[O:10]>O1CCCC1.C1(C)C=CC=CC=1>[CH:1]([CH:7]1[CH2:8][CH2:9][O:4][C:5](=[O:10])[CH2:6]1)=[CH2:2]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A stream of nitrogen gas is passed through a mixture of 19.6 mL (41.2 mmol) of 2.1M vinyllithium in tetra-hydrofuran and 21 mL toluene to evaporate tetrahydrofuran. The resulting pale yellow suspension is diluted with 21 mL ether and cooled to -78°. To this solution is added 1.87 g (20.9 mmol) cuprous cyanide and the reaction mixture is then warmed to 0° for 2 minutes. The resulting gray suspension is cooled to -78° and 0.9 mL (10.4 mmol) of 5,6-dihydro-2H-pyran-2-one is added. The reaction mixture is stirred at -78° for 30 minutes and at -20° for 15 minutes. The reaction is quenched by the addition of saturated aqueous ammonium chloride and stirred for 1 hour at room temperature. The insoluble salts are filtered off and washed with water (1×20 mL) and ether (2×20 mL). The layers are separated and the aqueous phase is extracted with ether (2×30 mL). Combined organic extracts are dried (MgSO4), filtered and evaporated to give yellow oil which is purified by flash chromatography to obtain 4-ethenyltetrahydro-2H-pyran-2-one as a pale yellow oil.
Workup
- customto evaporate tetrahydrofuran
- additionThe resulting pale yellow suspension is diluted with 21 mL ether
- temperaturecooled to -78°
- temperaturethe reaction mixture is then warmed to 0° for 2 minutes
- temperatureThe resulting gray suspension is cooled to -78°
- customThe reaction is quenched by the addition of saturated aqueous ammonium chloride
- stirringstirred for 1 hour at room temperature
- filtrationThe insoluble salts are filtered off
- washwashed with water (1×20 mL) and ether (2×20 mL)
- customThe layers are separated
- extractionthe aqueous phase is extracted with ether (2×30 mL)
- dry with materialCombined organic extracts are dried (MgSO4)
- filtrationfiltered
- customevaporated
- customto give yellow oil which
- customis purified by flash chromatography
Sources & evidence
- ORD record
- ord-3bdcff660a174df48ee60bf1bb3c17cb
- Source dataset
- uspto-grants-1991_06
- Patent number
- US05025025
Reaction notes
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