Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 839406Generated: October 26, 2026

Hydrochloric Acid → 3-Mercapto-4-cyclohexylphenylglyoxylic acid

https://huagongshe.com/reaction/839406

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 6N 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 numberUS04094995
Source datasetuspto-grants-1978_06
ORD IDord-a17d76013d4c4df1a4a5782dff5a8f9e
Source noteuspto-grants-1978_06