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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696285Generated: October 30, 2026

Hydrochloric Acid → Ethyl 1-acetyl-5-(cyclohexylmethyl)piperidine-3-carboxylate

https://huagongshe.com/reaction/1696285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantEthyl 5-(cyclohexylmethyl)piperidine-3-carboxylateHCID 66844627—
SolventDichloromethaneHCID 6344—
ProductEthyl 1-acetyl-5-(cyclohexylmethyl)piperidine-3-carboxylateHCID 66844834—

Reaction Steps

Triethylamine (410 μL, 2.9 mmol) was added to a solution of ethyl 5-(cyclohexylmethyl)piperidine-3-carboxylate (180 mg, 0.71 mmol) and acetyl chloride (120 mg, 1.4 mmol) in CH2Cl2 (10 mL). The reaction was maintained at room temperature for 30 min before being diluted with CH2Cl2 (20 mL) and poured into HCl (1 N, 20 mL). The layers were separated and the aqueous layer was extracted with CH2Cl2 (3×20 mL). The combined organic layers were sequentially washed with H2O (10 mL) and brine before being dried over Na2SO4. Concentration under reduced pressure and purification by silica gel chromatography (hexane→80% EtOAc/hexane) provided the title compound as a yellow oil. MS m/z: 296.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163766B2
Source datasetuspto-grants-2012_04
ORD IDord-ff1dad69d0334471b90cb9ecf74a01cf
Source noteuspto-grants-2012_04