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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1825898Generated: October 30, 2026

Potassium Carbonate → Hydrochloric Acid

https://huagongshe.com/reaction/1825898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPivaloyl chlorideHCID 62493—
ReactantHCID 12052823HCID 12052823—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHydrochloric AcidHCID 313—
ProductHCID 12052816HCID 12052816—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 0.08 g of potassium carbonate (0.58 mmol) in 1 ml. of water was added a solution of 0.20 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 0.075 g of trimethylacetyl chloride (0.62 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. 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.0.25 hydrate salt of the title compound with isopropanolic HCl to yield 0.157 g (58%) of white solid; mp=233–236° C.; MS (+) ESI m/z=429 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07049330B2
Source datasetuspto-grants-2006_05
ORD IDord-f992fa2a18bd4a76acfd36b5904add2f
Source noteuspto-grants-2006_05