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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199047Generated: November 1, 2026

Ethanol → HCID 19867685, compound

https://huagongshe.com/reaction/1199047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantEthyl 3-bromopropionateHCID 68320—
ReactantNanofinHCID 68843—
ProductHCID 19867685HCID 19867685—

Reaction Steps

A mixture of ethyl 3-bromo-propionate(25.8g), 2,6-dimethyl-piperidine (30 g) and ethanol (40 cc) is heated for 2 hours under reflux. The reaction mixture is concentrated to dryness under reduced pressure (2.7 kPa) and the residue is taken up in 5N sodium hydroxide solution (30 cc) and then extracted with methylene chloride (3×50 cc). The organic phase is dried over magnesium sulphate, filtered, and concentrated to dryness under reduced pressure (2.7 kPa) at 40° C. Ethyl 4-(2,6-dimethyl-1-piperidyl)butyrate(29 g) is thus obtained as an oil which can be employed in the subsequent synthesis without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04898871
Source datasetuspto-grants-1990_02
ORD IDord-2f9f50033a0143e4bc5430bce7c0cfe0
Source noteuspto-grants-1990_02