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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647043Generated: October 26, 2026

Hydrochloric Acid → HCID 12906149, compound

https://huagongshe.com/reaction/647043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium nitrosodisulfonateHCID 3032624—
ReactantHCID 12906148HCID 12906148—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
ProductHCID 12906149HCID 12906149—

Reaction Conditions

Temperature20 °C

Reaction Steps

5-(2'-Hydroxy-3',4',6'-trimethylbenzoyl)pentanoic acid (formula II-1 wherein R=H3C, X=H, Y=OH, n=4, in the free form) (0.048 part) was dissolved in 0.5% NaOH (3.3 volume parts) and, while the solution was stirred at 20° C., potassium nitrosodisulfonate (0.4 part) was added. The mixture was stirred for 10 minutes. Then, under cooling with ice, the reaction mixture was diluted with water (100 volume parts) and rendered acidic with dilute hydrochloric acid. It was then extracted with diethyl ether and the extract was washed with water and dried. The solvent was distilled off under reduced pressure and the residue was then recrystallized from hexane-ethyl acetate (2:1). The procedure provided 2,3,5-trimethyl-6-(5'-carboxy-1'-oxopentyl)-1,4-benzoquinone (formula I-1 wherein R=H3C, n=4, in the free form) (0.042 part) as yellow needles melting at 96.5°-98.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04407757
Source datasetuspto-grants-1983_10
ORD IDord-b848c61be6a84839927606acc4fb8798
Source noteuspto-grants-1983_10