Water → 1-[3-(3,4-Dimethoxyphenyl)piperidin-1-yl]propan-1-one
Reaction equation
C(=O)([O-])[O-].[Na+].[Na+].[CH3:7][O:8][C:9]1[CH:10]=[C:11]([CH:17]2[CH2:22][CH2:21][CH2:20][NH:19][CH2:18]2)[CH:12]=[CH:13][C:14]=1[O:15][CH3:16].[C:23](Cl)(=[O:26])[CH2:24][CH3:25].O>O1CCCC1>[C:23]([N:19]1[CH2:20][CH2:21][CH2:22][CH:17]([C:11]2[CH:12]=[CH:13][C:14]([O:15][CH3:16])=[C:9]([O:8][CH3:7])[CH:10]=2)[CH2:18]1)(=[O:26])[CH2:24][CH3:25]Participants
Procedure
260 mg of sodium carbonate were added under a nitrogen atmosphere to a mixture of 500 mg of 3-(3',4'-dimethoxyphenyl)-piperidine in 5 ml of tetrahydrofuran and while cooling the mixture on an ice bath, 0.21 ml of propionyl chloride was added dropwise over 5 minutes. After the temperature rose to room temperature, the mixture was stirred for 11/2 hours and was then poured into 10 volumes of ice and water. The mixture was extracted with methylene chloride and the extracts were washed with water, dried over magnesium sulfate and evaporated to dryness under reduced pressure. The 460 mg of residue was chromatography over silica gel and was eluted with a 6-3-1 cyclohexane-chloroform-triethylamine mixture. The product was crystallized to get 270 mg of amorphous N-propionyl-3-(3',4'-dimethoxyphenyl)-piperidine.
Workup
- temperaturewhile cooling the mixture on an ice bath
- customrose to room temperature
- extractionThe mixture was extracted with methylene chloride
- washthe extracts were washed with water
- dry with materialdried over magnesium sulfate
- customevaporated to dryness under reduced pressure
- washwas eluted with a 6-3-1 cyclohexane-chloroform-triethylamine mixture
- customThe product was crystallized
Sources & evidence
- ORD record
- ord-a956ff170a57476a8c7356b6117f6249
- Source dataset
- uspto-grants-1978_02
- Patent number
- US04072685
Reaction notes
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