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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104231Generated: October 30, 2026

Hydrochloric Acid → 1-(Tert-butoxycarbonyl)-4-(4-chlorophenyl)piperidine-4-carboxylic acid

https://huagongshe.com/reaction/2104231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(4-Chloro-phenyl)-piperidine-4-carboxylic acid hydrochlorideHCID 69049732—
SolventWaterHCID 962—
Product1-(Tert-butoxycarbonyl)-4-(4-chlorophenyl)piperidine-4-carboxylic acidHCID 24828857—

Reaction Steps

A sample of crude 4-(4-chloro-phenyl)-piperidine-4-carboxylic acid hydrochloride (5 mmol, 1 equiv) and 15 g of K2CO3 (113 mmol, 22.6 equiv) was diluted in 50 mL H2O. To the resultant solution was added a solution of 7.4 g BOC20 (34.1 mmol, ˜7 equiv) in 50 mLp-dioxane and the reaction mixture was stirred overnight under N2 atmosphere. The pH was adjusted to ˜4 with 1M HCl and allowed to stir for about 0.5 hour. The reaction mixture was concentrated under vacuum, and the remaining solution was extracted with 2×50 mL EtOAc. The combined organic extracts were dried under vacuum to yield 4-(4-chloro-phenyl)-piperidine-1,4-dicarboxylic acid mono-tert-butyl ester. The crude material was used without further purification for the next step: MS (ES) M−H expected=338.8, found=338.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576218B2
Source datasetuspto-grants-2009_08
ORD IDord-4c02b82ce9464db8985752374cd7268e
Source noteuspto-grants-2009_08