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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783609Generated: November 1, 2026

Methyl chloroformate → HCID 61056118, compound

https://huagongshe.com/reaction/1783609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantTriethylamineHCID 8471—
Reactant4-Aminopiperidine-4-carboxylic acid--hydrogen chloride (1/2)HCID 22907088—
SolventTetrahydrofuranHCID 8028—
ProductHCID 61056118HCID 61056118—

Reaction Conditions

Temperature0 °C

Reaction Steps

(1-Methyl-4-methylamino-piperidin-4-yl)-methanol is prepared from 4-amino-piperidine-4-carboxylic acid 2 HCl. Methyl chloroformate (0.40 g, 4.2 mmol) is added dropwise to a mixture of 4-amino-piperidine-4-carboxylic acid 2 HCl (0.278 g, 1.28 mmol) and Et3N (0.713 g, 7.04 mmol) in THF (10 ml) at room temperature. After 16 h, the reaction mixture is filtered, rinsed with EtOAc and concentrated. A solution of LAH in THF (5 ml of a 1 M solution) is added to the residue. After stirring at reflux for 4 h, the reaction mixture is cooled to 0° C. and carefully quenched with Na2SO4.10H2O. After warming to room temperature the reaction mixture is diluted with EtOAc and filtered through Celite. The filtrate is concentrated to give (1-methyl-4-methylamino-piperidin-4-yl)-methanol which is carried forward without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501427B2
Source datasetuspto-grants-2009_03
ORD IDord-9cbd597be3574ea3adaec85f4b538689
Source noteuspto-grants-2009_03