Allyl bromide → HCID 23396873, compound
Reaction equation
[Li+].CC([N-][CH:6]([CH3:8])[CH3:7])C.[CH2:9]([O:16][C:17]([CH:19]1[CH2:23][CH2:22][CH2:21][CH2:20]1)=[O:18])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.C(Br)C=C>C1COCC1>[CH2:9]([O:16][C:17]([C:19]1([CH2:8][CH:6]=[CH2:7])[CH2:23][CH2:22][CH2:21][CH2:20]1)=[O:18])[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- -78 °C
Procedure
Next, to a stirred solution of LDA (4 mmol, 2M in Hexane) in THF (8 mL) at −78° C. is added a solution of cyclopentanecarboxylic acid benzyl ester (817 mg, 4 mmol) in THF (3 mL) dropwise. After the addition, the mixture is stirred at −78° C. for 5 hours then allyl bromide (726 mg, 6 mmol) is added dropwise. The mixture is warmed to room temperature during 4 hours then the reaction mixture is quenched with saturated NaHCO3. Magnesium sulfate (2 g) is added and stirred until all the MgSO4 is dissolved. The mixture is extracted with ethyl acetate and the organic layer is washed with water, brine, dried over MgSO4 and filtered. The solvent is removed under reduced pressure and the residue is purified by flash chromatography (hep:EtOAc, 10:1) to give 1-allyl-cyclopentanecarboxylic acid benzyl ester.
Workup
- additionAfter the addition
- temperatureThe mixture is warmed to room temperature during 4 hours
- customthe reaction mixture is quenched with saturated NaHCO3
- additionMagnesium sulfate (2 g) is added
- stirringstirred until all the MgSO4
- dissolutionis dissolved
- extractionThe mixture is extracted with ethyl acetate
- washthe organic layer is washed with water, brine
- dry with materialdried over MgSO4
- filtrationfiltered
- customThe solvent is removed under reduced pressure
- customthe residue is purified by flash chromatography (hep:EtOAc, 10:1)
Sources & evidence
- ORD record
- ord-e97eda5e7f864208a094ceda7c096f9d
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08263629B2
Reaction notes
Loading…