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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059326Generated: October 31, 2026

Hydrochloric Acid → HCID 18670134, compound

https://huagongshe.com/reaction/1059326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 18670486HCID 18670486—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18670134HCID 18670134—

Reaction Steps

To a solution of 6.7 g of 4-[1-(tert-butoxycarbonyl)-piperidin-4-yl]-3,3-dimethylbutyronitrile in 50 ml of tetrahydrofuran was added at room temperature 20 ml of conc. hydrochloric acid and the resulting mixture was stirred for 2 hours. Then the reaction mixture was concentrated under reduced pressure to thereby give crude 4-(piperidin-4-yl)-3,3-dimethylbutyronitrile hydrochloride. This crude product was dissolved in 100 ml of dichloromethane. After adding 10.5 g of anhydrous potassium carbonate and 3.3 ml of benzyl bromide, the reaction mixture was reacted at room temperature for 12 hours. After adding water, the reaction mixture was extracted with ethyl acetate, washed with a saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate. After distilling off the solvent under reduced pressure, the residue was purified by silica gel column chromatography (eluted with n-hexane/ethyl acetate) to thereby give 4.7 g of the title compound as a colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06518423B1
Source datasetuspto-grants-2003_02
ORD IDord-09a1a6309d404de99f46962498d68370
Source noteuspto-grants-2003_02