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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301746Generated: October 25, 2026

Hydrochloric Acid → Benzyl 4-(methoxycarbonylamino)piperidine-1-carboxylate

https://huagongshe.com/reaction/2301746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantBenzyl 4-isocyanatopiperidine-1-carboxylateHCID 2776273—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductBenzyl 4-(methoxycarbonylamino)piperidine-1-carboxylateHCID 18677680—

Reaction Steps

To a solution of 1.0 g (3.9 mmol) of (1-benzyloxycarbonylpiperidin-4-yl)isocyanate from Procedure 1, Step A in 10 mL of methanol was added 5 mg (cat) of DMAP. The reaction was stirred under nitrogen at rt for 24 h and then poured into water containing 2 mL of 2 N hydrochloric acid and was extracted twice with ethyl acetate. The organic layers were each washed with a portion of brine, dried over sodium sulfate, combined and concentrated to give 1.4 g of the crude title compound which can be used directly in subsequent reactions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500844B1
Source datasetuspto-grants-2002_12
ORD IDord-b93f0b6bd0254345ad23d45c2ab44154
Source noteuspto-grants-2002_12