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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881682Generated: October 30, 2026

Acetyl chloride → Methyl 4-(piperidin-2-yl)butanoate hydrochloride

https://huagongshe.com/reaction/1881682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTert-butyl 2-(4-methoxy-4-oxobutyl)piperidine-1-carboxylateHCID 57904248—
SolventMethanolHCID 887—
ProductMethyl 4-(piperidin-2-yl)butanoate hydrochlorideHCID 66772062100%

Reaction Steps

Acetyl chloride was slowly added dropwise to a solution of tert-butyl 2-(4-methoxy-4-oxobutyl)piperidine-1-carboxylate (3) (25.67 g, 89.9 mmol) in methanol. The reaction mixture was stirred at room temperature for 5 h. The complete reaction was checked by means of TLC. When the reaction was complete, the reaction mixture was concentrated under reduced pressure to obtain methyl 4-(piperidine-2-yl)butanoate hydrochloride (4) (20.14 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318769B2
Source datasetuspto-grants-2012_11
ORD IDord-3609fd042a8b433fad0ebe890b2cccec
Source noteuspto-grants-2012_11