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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165358Generated: November 1, 2026

Hydrochloric Acid → HCID 19862973, compound

https://huagongshe.com/reaction/1165358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 19862974HCID 19862974—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 19862973HCID 19862973—

Reaction Steps

To the above 1-carbobenzoxymethyl-1-carbomethoxyethylcyclohexane (40.4 g) in dioxane (300 ml) was added 1N NaOH (150 ml) dropwise over 2 hours with stirring at room temperature. After 6 hours the reaction was neutralized with 1N HCl then the dioxane was evaporated. The cloudy solution was diluted with water, acidified with 1N HCl, then extracted two times with ethyl acetate, washed with saturated NaCl (aqueous), dried with MgSO4, filtered and then concentrated to an oil. By 1H NMR no mono-methyl ester could be seen in the crude reaction mixture, the major by product being the di-acid. The product was purified by flash chromatography (silica gel, eluted with CHCl3, MeOH,HOAc 99:1:0.1) then distilled free of the residual benzyl alcohol to give 1-carbobenzoxymethyl-1-carboxyethylcyclohexane. (29.6 g, 76%) 1H-NMR (CDCl3): δ7.05(s,5H); 4.9(s,2H); 2.35-2.1(m,2H); 2.2(s,2H); 1.85-1.55(m,2H); 1.35(br s,10H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04908475
Source datasetuspto-grants-1990_03
ORD IDord-1f6416ab31ef44d19c8e0aae6ecc6fea
Source noteuspto-grants-1990_03