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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716516Generated: October 26, 2026

Piperidine → (1-Thiocarbamoylpiperidin-4-yl)acetic acid tert-butyl ester

https://huagongshe.com/reaction/1716516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantFmoc isothiocyanateHCID 4154759—
ReactantTert-butyl 2-(piperidin-4-yl)acetateHCID 23511620—
SolventChloroformHCID 6212—
Product(1-Thiocarbamoylpiperidin-4-yl)acetic acid tert-butyl esterHCID 58706572—

Reaction Steps

A solution of piperidin-4-ylacetic acid tert-butyl ester (10.72 g, 50.0 mmol) in chloroform (100 ml) was added to a solution of 9-fluorenylmethoxycarbonyl isothiocyanate (14.07 g, 50.0 mmol) in chloroform (100 ml) and the mixture was stirred at room temperature for 1 hour. Then, piperidine (80 ml) was added and the mixture was stirred at room temperature for 30 minutes. After the reaction solution was concentrated, water was added, and it was extracted with ethyl acetate and washed with a saturated brine. The organic layer was dried over magnesium sulfate and the residue obtained by vacuum concentration was washed with isopropyl ether and the title compound was obtained (11.35 g, 98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803801B2
Source datasetuspto-grants-2010_09
ORD IDord-0ca6a52373b042fbb4b75bbd76010b49
Source noteuspto-grants-2010_09