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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171658Generated: November 4, 2026

1,2-Dichloroethane → Piperidin-4-yl benzoate

https://huagongshe.com/reaction/2171658

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantBenzoyl chlorideHCID 7412—
ReactantSodium BicarbonateHCID 516892—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
SolventEthyl AcetateHCID 8857—
ProductPiperidin-4-yl benzoateHCID 12416427101.3%

Reaction Steps

tert-Butyl 4-hydroxypiperidine-1-carboxylate (3.0 g) was mixed with DCE (30 ml), and TEA (3.0 ml) and benzoyl chloride (2.4 g) was added thereto, followed by stirring at room temperature for 1 hour. A saturated aqueous sodium hydrogen carbonate solution and EtOAc were added to the reaction mixture, and the organic layer was dried over Na2SO4 and concentrated under reduced pressure. The obtained residue was mixed with DCE (30 ml), and TFA (10 ml) was added thereto, followed by stirring at room temperature for 5 hours. The reaction mixture was concentrated under reduced pressure, and then the residue was purified by basic silica gel column chromatography (CHCl3/MeOH) to obtain piperidin-4-yl benzoate (3.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051283B2
Source datasetuspto-grants-2015_06
ORD IDord-45af65e5dfc047deb55591d05b036400
Source noteuspto-grants-2015_06