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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696287Generated: November 2, 2026

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

https://huagongshe.com/reaction/1696287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantEthyl 5-(cyclohexylmethyl)piperidine-3-carboxylateHCID 66844627—
SolventDichloromethaneHCID 6344—
ProductEthyl 5-(cyclohexylmethyl)-1-(methylsulfonyl)piperidine-3-carboxylateHCID 66844753—

Reaction Conditions

Temperature0 °C

Reaction Steps

Triethylamine (340 mL, 2.4 mmol) was added to a solution of ethyl 5-(cyclohexylmethyl)piperidine-3-carboxylate (155 mg, 0.60 mmol) and methanesulfonyl chloride (75 mL, 0.90 mmol) in CH2Cl2 (6 mL) cooled to 0° C. The reaction was maintained at this temperature for 15 min at which point the whole was allowed to warm to RT and stir for an additional 3 h. The reaction was diluted with CH2Cl2 (20 mL) and poured into HCl (1N, 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 provided the title compound. MS m/z: 332.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163766B2
Source datasetuspto-grants-2012_04
ORD IDord-c7193180698c49389f1ccc104d8c9b6f
Source noteuspto-grants-2012_04