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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225486Generated: October 30, 2026

Hydrochloric Acid → 1-Methyl-4-oxocyclohexane-1-carboxylic acid

https://huagongshe.com/reaction/2225486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 1-methyl-4-oxocyclohexane-1-carboxylateHCID 12568255—
SolventMethanolHCID 887—
Product1-Methyl-4-oxocyclohexane-1-carboxylic acidHCID 2260994389.4%

Reaction Steps

50 ml of a 3N aqueous sodium hydroxide solution was added to a solution of 5 g of methyl 1-methyl-4-oxo-1-cyclohexanecarboxylate, which is disclosed in a literature [T. Sohda, K. Meguro, and Y. Kawamatsu, Chem. Pharm. Bull., 32, 2267-2278 (1984)], in 150 ml of methanol. The resultant solution was reacted for 2 hours, while it was refluxed. After reaction, 2N hydrochloric acid was added to the solution, acidifying the solution. The solution was extracted five times with 50 ml of ethyl acetate. The organic layer obtained was washed three times with an aqueous sodium chloride solution and was then dried over magnesium sulfate. Thereafter, the solvent was removed in vacuo. The oily substance obtained was subjected to column chromatography using 50 g of silica gel. From the fraction eluted with hexane and ethyl acetate=2:1, the solvent was removed in vacuo, yielding 4.1 g of 1-methyl-4-oxo-1-cyclohexanecarboxyic acid as a colorless oil, which had the following physiochemical properties:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05344845
Source datasetuspto-grants-1994_09
ORD IDord-d8796d02f91a4fa0a02ffefcb589aac1
Source noteuspto-grants-1994_09