Ethanol → HCID 13039291, compound

A mixture of 7.28 g of cis-4-(4-bromophenoxy)-1-ethoxycarbonyl-3-phenylpiperidine, 48 ml of 20% aqueous sodium hydroxide solution and 90 ml of absolute ethanol is refluxed overnight under nitrogen. The mixture is cooled and partitioned between 50 ml of water and 100 ml of ether. The aqueous phase is extracted with ether (100 ml), and the combined organic phases are concentrated in vacuo. The resulting solid is dissolved in dichloromethane (100 ml) and washed with saturated sodium chloride solution. After drying over anhydrous sodium sulfate, filtration and concentration in vacuo affords a nearly colorless solid. The solid is dissolved in 200 ml of boiling hexane and the solution is reduced after boiling down in volume to about 150 ml. The solution is filtered, allowed to cool to room temperature and refrigerated overnight to afford product as a nearly colorless, crystalline solid, mp. 113°-115° C.

1. temperatureis refluxed overnight under nitrogen
2. temperatureThe mixture is cooled
3. custompartitioned between 50 ml of water and 100 ml of ether
4. extractionThe aqueous phase is extracted with ether (100 ml)
5. concentrationthe combined organic phases are concentrated in vacuo
6. dissolutionThe resulting solid is dissolved in dichloromethane (100 ml)
7. washwashed with saturated sodium chloride solution
8. dry with materialAfter drying over anhydrous sodium sulfate, filtration and concentration in vacuo
9. customaffords a nearly colorless solid
10. filtrationThe solution is filtered
11. customto afford product as a nearly colorless, crystalline solid, mp. 113°-115° C.

ORD record

ord-8df4a15a5a2a4a0fafcd11a05c0833e4

Source dataset

uspto-grants-1983_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04382141