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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351550Generated: October 26, 2026

Benzyl 4-(methoxy(methyl)carbamoyl)piperidine-1-carboxylate → Benzyl 4-acetylpiperidine-1-carboxylate

https://huagongshe.com/reaction/1351550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 4-(methoxy(methyl)carbamoyl)piperidine-1-carboxylateHCID 22574154—
ReactantHCID 178418573HCID 178418573—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl 4-acetylpiperidine-1-carboxylateHCID 19065050—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 5 g of 4-(N-methoxy-N-methyl-carbamoyl)-piperidine-1-carboxylic acid benzyl ester (S. Nahm and S. W. Weinreb, Tetrahedron Letters, 22:3815–3818(1981)) in 50 mL of anhydrous THF cooled to 0° C., was added dropwise 6 mL of 3M methylmagnesium bromide in ether over 10 minutes. After stirring for 1 h at 0° C., the resulting mixture was quenched with 50 mL of 1N HCl and extracted with 3×50 mL of ether. The combined extracts were dried over magnesium sulfate and concentrated to dryness under reduced pressure. Drying under vacuum gave 4-Acetyl-piperidine-1-carboxylic acid benzyl ester as a white solid:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217716B2
Source datasetuspto-grants-2007_05
ORD IDord-00c25f69a5a9475cae5d6e5ff53cfea5
Source noteuspto-grants-2007_05