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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633889Generated: October 30, 2026

Acetyl chloride → Tert-butyl 2-(5-methyl-1,2,4-oxadiazol-3-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/633889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-butyl 2-[(Z)-N'-hydroxycarbamimidoyl]piperidine-1-carboxylateHCID 45833400—
SolventAcetonitrileHCID 6342—
ProductTert-butyl 2-(5-methyl-1,2,4-oxadiazol-3-yl)piperidine-1-carboxylateHCID 6833814333.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

In a 16 mL vial, tert-butyl 2-[(Z)-amino(hydroxyimino)methyl]piperidine-1-carboxylate (150 mg, 0.62 mmol; which may be prepared as described in Step 1) was dissolved in acetonitrile (6.2 mL) and cooled at 0° C. under nitrogen. DIPEA (324 μL, 1.86 mmol) and acetyl chloride (88 μL, 1.24 mmol) were added dropwise and the reaction mixture was allowed to warm to room temperature then heated to 100° C. for 4 h, cooled and concentrated. The residue was taken up in EtOAc and water. The two layers were separated and the aqueous phase extracted with EtOAc. The combined organics were dried on Na2SO4 and concentrated. The residue was taken up in o-xylene (7 mL) and heated to 150° C. for 3 h then concentrated. The crude mixture was purified on column chromatography (eluent: Pentane/EtOAc 7/3) to give the product (55 mg, 33%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321769B2
Source datasetuspto-grants-2016_04
ORD IDord-dc44500afe0a4a4fa0973b507d362234
Source noteuspto-grants-2016_04