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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842635Generated: November 1, 2026

Potassium Carbonate → Hydrochloric Acid

https://huagongshe.com/reaction/842635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Methylcyclohexanecarbonyl chlorideHCID 4189245—
ReactantHCID 12052823HCID 12052823—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHydrochloric AcidHCID 313—
ProductHCID 12052814HCID 12052814—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 0.08 g of potassium carbonate (0.58 mmol) in 1 ml. of water 1o was added a solution of 0.18 g of {(1R)-1-cyclohexylmethyl-2-[4-(2-methoxyphenyl)-piperidin-1-yl]-ethyl}-methyl-amine (0.58 mmol) in 10 mL of dichloromethane. The resulting mixture was cooled to 0° C. and 0.093 g of 1-methyl -cyclohexanecarboxylic acid chloride (0.58 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 0.220 g (75%) of white solid; mp=169-171° C.; MS(+)ESI m/z=469 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376494B1
Source datasetuspto-grants-2002_04
ORD IDord-1edb871eff2147bea4eadbe74e0a3ed5
Source noteuspto-grants-2002_04