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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570105Generated: October 30, 2026

Methanol → 1-Methoxy-4-methylamino-piperidine-4-carboxylic acid methyl ester

https://huagongshe.com/reaction/570105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantThionyl ChlorideHCID 24386—
Reactant1-Methoxy-4-methylamino-piperidine-4-carboxylic acidHCID 58537906—
Product1-Methoxy-4-methylamino-piperidine-4-carboxylic acid methyl esterHCID 58537903—

Reaction Steps

To a suspension of 1-methoxy-4-methylamino-piperidine-4-carboxylic acid (2.0 g, 10.63 mmol) in methanol (50 ml) at 0-10° C. was added thionyl chloride (2.29 ml, 3.76 g, 31.57 mmol) and the reaction mixture was heated at reflux overnight. 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 ethyl acetate (4×25 ml) and dichloromethane (4×50 ml), the combined organic layers washed with aqueous sodium bicarbonate (15 ml) and brine (15 ml), dried over sodium sulfate and concentrated. Yield: 0.76 g of 1-methoxy-4-methylamino-piperidine-4-carboxylic acid methyl ester (compound P5.4) as a viscous, orange oil. The spectral data of this crude material were identical to those described above under preparation example 6, step 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023760B2
Source datasetuspto-grants-2015_05
ORD IDord-9c3617cb09e54e2b90b54d0e61c8f534
Source noteuspto-grants-2015_05