Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444570Generated: October 26, 2026

Hydrochloric Acid → 3-Mercapto-4-cyclohexylphenylglyoxylic acid

https://huagongshe.com/reaction/444570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium ethylxanthateHCID 2735045—
ReactantEthyl 3-amino-4-cyclohexylphenylglyoxylateHCID 20515218—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product3-Mercapto-4-cyclohexylphenylglyoxylic acidHCID 20515165—

Reaction Steps

To 17.3 g. of ethyl 3-amino-4-cyclohexylphenylglyoxylate in 11.1 ml. of concentrated hydrochloric acid and 20 g. of ice is added 4.1 g. of sodium nitrite in 2 ml. of water. This mixture is stirred for 10 min. and then added gradually to an ice cold solution of 10.3 g. of potassium ethyl xanthate in 14 ml. of water. The reaction is gradually heated over 45 minutes to 50° C. and stirred an additional 45 minutes. The mixture is then cooled, extracted with ether which is then washed with water, dilute sodium hydroxide and water, dried over sodium sulfate and evaporated in vacuo. The residue is dissolved in 35 ml. of boiling ethanol to which is added gradually 13 g. of potassium hydroxide. The reaction is refluxed an additional hour and then evaporated to dryness in vacuo. The residue is dissolved in water and extracted with ether. The alkaline phase is acidified with 6 N sulfuric acid and extracted with ether. The ether is washed with water, dried over sodium sulfate and evaporated to dryness to obtain 3-mercapto-4-cyclohexylphenylglyoxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04264627
Source datasetuspto-grants-1981_04
ORD IDord-2d56c9f3a7a14627b259ace44ee34680
Source noteuspto-grants-1981_04