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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1409549Generated: October 25, 2026

4-Aminotetrahydro-2H-pyran-4-carboxylic acid hydrochloride → Methyl 4-aminooxane-4-carboxylate

https://huagongshe.com/reaction/1409549

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Aminotetrahydro-2H-pyran-4-carboxylic acid hydrochlorideHCID 2734400—
Reactanttrimethylsilyldiazomethane Et2OHCID 23159941—
SolventMethanolHCID 887—
ProductMethyl 4-aminooxane-4-carboxylateHCID 1869831499%

Reaction Steps

To a solution of 4-amino-4-carboxy-tetrahydropyrane hydrochloride (2 g) in methanol was added dropwise a solution of 2M trimethylsilyldiazomethane-diethylether (33 mL) under ice-cooling, and the mixture was stirred at room temperature for 4 days. The reaction mixture was concentrated in vacuo, and the resultant crude product was dissolved in hexane-diethylether (1 mL/1 mL), and thereto was added an aqueous 4N hydrochloric acid. The precipitates were collected by filtration to give 4-amino-4-methoxycarbonyl-tetrahydropyrane (2.13 g, yield: 99%) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921380B2
Source datasetuspto-grants-2014_12
ORD IDord-c6845010739e41f19e1c9c8429a37b52
Source noteuspto-grants-2014_12