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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1535023Generated: October 26, 2026

Hydrochloric Acid → (1-Nitromethylcyclohexyl)acetic acid ethyl ester

https://huagongshe.com/reaction/1535023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantNitromethaneHCID 6375—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl cyclohexylideneacetateHCID 73776—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product(1-Nitromethylcyclohexyl)acetic acid ethyl esterHCID 1112808388.4%

Reaction Steps

To a mixture of 64.72 g (0.469 mole) potassium carbonate suspended in 469.5 mL dimethyl sulphoxide is measured in, during the course of 1 to 2 hours at 95° C., a solution of 158 g, (0.939 mole) ethyl cyclohexylideneacetate and 85.94 g (1.408 mole) nitromethane. After completion of the addition, stirring is continued at 95° C. for 2 to 3 hours. Subsequently, with ice-water cooling, the reaction solution is acidified with about 150 mL concentrated hydrochloric acid and diluted with 1.5 L of water. The resultant phases are separated and the aqueous phase is extracted several times with petroleum ether. The combined organic phases are washed neutral with water and dried over anhydrous sodium sulphate. The solvent is subsequently distilled off in a vacuum. 190.3 g Ethyl 1-nitromethyl-cyclohexaneacetate in the form of an oil are obtained; yield 88.4% of theory. Composition according to HPLC: 90% of the desired product of Step 2 and 6% ethyl cyclohexylideneacetate (Step 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05091567
Source datasetuspto-grants-1992_02
ORD IDord-27f300d0b40b444a9599d3f111d4e69c
Source noteuspto-grants-1992_02