Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298084Generated: October 29, 2026

Tert-butyl 4-iodopiperidine-1-carboxylate → HCID 53748621, compound

https://huagongshe.com/reaction/2298084

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-iodopiperidine-1-carboxylateHCID 10892302—
ReactantBenzenesulfonothioic acid, 4-methyl-, potassium salt (1:1)HCID 23662126—
SolventEthanolHCID 702—
ProductHCID 53748621HCID 5374862141.9%

Reaction Steps

4-Iodo-piperidine-1-carboxylic acid, tert-butyl ester (1.3 g) and potassium toluene-4-thiosulfonate (1.0 g) were combined in ethanol (10 ml) with cis-dicyclohexane 18-crown-6 (10 mg) and heated under reflux for 12 h. After cooling the reaction mixture was partitioned between ethyl acetate and water, the organic layer was separated, washed with water and brine, dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel chromatography (eluting with iso-hexane/ethyl acetate 4:1 to 7:3), to yield the subtitle compound as an oil (0.65 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492355B1
Source datasetuspto-grants-2002_12
ORD IDord-21bced64890145c488b6e1c9cf0cab0a
Source noteuspto-grants-2002_12