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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473791Generated: October 30, 2026

Methanol → 4-Hydroxyamino-1-methoxy-piperidine-4-carboxylic acid methyl ester

https://huagongshe.com/reaction/1473791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantThionyl ChlorideHCID 24386—
Reactant4-Hydroxyamino-1-methoxy-piperidine-4-carboxylic acidHCID 86657467—
Product4-Hydroxyamino-1-methoxy-piperidine-4-carboxylic acid methyl esterHCID 86657465—

Reaction Steps

To a suspension of 4-hydroxyamino-1-methoxy-piperidine-4-carboxylic acid (1.0 g, 5.26 mmol) in methanol (25 ml) at 0-10° C. was added thionyl chloride (1.14 ml, 1.88 g, 15.77 mmol) and the reaction mixture was heated at reflux for 48 hours. After cooling, the mixture was concentrated, the residue diluted with ice water (20 ml) and neutralised with aqueous sodium bicarbonate. The aqueous phase was extracted with diethyl ether (3×25 ml), the combined organic layers washed with aqueous sodium bicarbonate and brine, dried over sodium sulfate and concentrated. Yield: 0.53 g of 4-hydroxyamino-1-methoxy-piperidine-4-carboxylic acid methyl ester (title compound P4ii.2) as a viscous, yellowish oil. This material was identical to the compound described above under preparation ‘EXAMPLE 11, Step 3’.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018135B2
Source datasetuspto-grants-2015_04
ORD IDord-c412afc450e244a89538b18655c3584a
Source noteuspto-grants-2015_04