Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593006Generated: November 1, 2026

Acetyl chloride → 4-(3-Methyl-1,2,4-oxadiazol-5-yl)piperidine hydrochloride

https://huagongshe.com/reaction/1593006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant1,1-Dimethylethyl 4-(3-methyl-1,2,4-oxadiazol-5-yl)-1-piperidinecarboxylateHCID 21098360—
SolventMethanolHCID 887—
Product4-(3-Methyl-1,2,4-oxadiazol-5-yl)piperidine hydrochlorideHCID 4579188855%

Reaction Conditions

Temperature60 °C

Reaction Steps

Crude tert-butyl 4-(3-methyl-1,2,4-oxadiazol-5-yl)piperidine-1-carboxylate (5.73 g, 21.3 mmol) was dissolved in MeOH (100 mL) and a premixed solution of acetyl chloride (1.53 mL, 42.8 mmol) in MeOH (10 mL) was added and the mixture heated to 60° C. for 1 hour, then the solvents were evaporated and the resultant gum triturated with dichloromethane/diethyl ether (1:1) to give a cream solid which was filtered, washed with diethyl ether and dried, to give the title compound as a solid (1.98 g, 55% yield); MS: 168 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07294636B2
Source datasetuspto-grants-2007_11
ORD IDord-b51cf27fcf4f48e2be4bf1cc431a7188
Source noteuspto-grants-2007_11