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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842633Generated: October 30, 2026

Potassium Carbonate → Hydrochloric Acid

https://huagongshe.com/reaction/842633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Methylcyclohexanecarbonyl chlorideHCID 4189245—
ReactantHCID 12052822HCID 12052822—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHydrochloric AcidHCID 313—
ProductHCID 12052812HCID 12052812—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 0.076 g of potassium carbonate (0.54 mmol) in 1 ml. of water was added a solution of 0.18 g of {(1R)-1-cyclohexylmethyl-2-[4-(2-methoxyphenyl)-piperidin-1-yl]-ethyl}-amine (0.54 mmol) in 10 mL of dichloromethane. The resulting mixture was cooled to 0° C. and 0.085 g of 1-methyl -cyclohexanecarbonyl chloride (0.54 mmol) was added. The reaction was allowed to stir overnight at 0° C., and was then diluted with 5 mL of water and 20 mL of dichloromethane and the phases separated. The aqueous phase was extracted with three additional portions of dichloromethane, and the combined organic phases were dried over anhydrous sodium sulfate, filtered and concentrated on a rotary evaporator to yield the crude product, which was purified by flash chromatography on silica gel (dichloromethane/methanol) and converted to the hydrochloride. 0.75 hydrate salt of the title compound with isopropanolic HCl to yield 0.35 g (55%) as a white solid; mp=208-210° C.; MS(+)ESI m/z=455 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376494B1
Source datasetuspto-grants-2002_04
ORD IDord-95435daaf87d4d26a7eda6f1de1bc29a
Source noteuspto-grants-2002_04