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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873828Generated: November 2, 2026

Tetrahydrofuran → 4-Acetyl-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1873828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactanttert-Butyl 4-(methoxy(methyl)carbamoyl)piperidine-1-carboxylateHCID 11065582—
ReactantHCID 178420676HCID 178420676—
SolventDiethyl EtherHCID 3283—
Product4-Acetyl-piperidine-1-carboxylic acid tert-butyl esterHCID 10987983—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 500 ml round bottom flask was added tert-butyl-4-{[methoxy(methyl)amino]carbonyl}piperidine-1-carboxylate (29 g, 106 mmol) and 150 ml tetrahydrofuran. The resulting solution was cooled with ice bath and methylmagnesium chloride tetrahydrofuran solution (42.6 ml, 3M, 128 mmol) was added by a syringe. The mixture was stirred at 0° C. for 30 minutes. It was diluted with 200 ml of ether and the resulting mixture was washed twice with 150 ml saturated ammonium chloride solution. The organics were dried over sodium sulfate, filtered and concentrated. The crude product was used for next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304434B2
Source datasetuspto-grants-2012_11
ORD IDord-cc4d041e11924b0daa6ad96abe7f9312
Source noteuspto-grants-2012_11