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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534949Generated: October 29, 2026

Hydrochloric Acid → 1-{[4-(2-Tert-butylphenyl)piperazin-1-yl](oxo)acetyl}piperidine-4-carboxylic acid

https://huagongshe.com/reaction/534949

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium HydroxideHCID 3939—
ReactantMethyl 1-{[4-(2-tert-butylphenyl)piperazin-1-yl](oxo)acetyl}piperidine-4-carboxylateHCID 66751159—
SolventTetrahydrofuranHCID 8028—
Product1-{[4-(2-Tert-butylphenyl)piperazin-1-yl](oxo)acetyl}piperidine-4-carboxylic acidHCID 6675132496%

Reaction Steps

To a stirred solution of methyl 1-{[4-(2-tert-butylphenyl)piperazin-1-yl](oxo)acetyl}piperidine-4-carboxylate (Example 88, 0.159 g, 0.383 mmol) in THF (3 mL) stirring at 0° C. was added 1 M lithium hydroxide solution (3 mL, 3 mmol). After 2 h the reaction mixture was acidified with 1 M hydrochloric acid solution and extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO4, and the solvent was evaporated under reduced pressure to provide 1-{[4-(2-tert-butylphenyl)piperazin-1-yl](oxo)acetyl}piperidine-4-carboxylic acid (0.147 g, 96%) as a white amorphous.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853215B2
Source datasetuspto-grants-2014_10
ORD IDord-0cd27e077c52466c80485f1caf7250c6
Source noteuspto-grants-2014_10