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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647052Generated: October 31, 2026

Hydrochloric Acid → 2,3,5-Trimethyl-6-(5'-carboxy-1'-hydroxypentyl)-1,4-benzoquinone

https://huagongshe.com/reaction/647052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantPotassium nitrosodisulfonateHCID 3032624—
Reactant6-Hydroxy-6-(2'-hydroxy-3',4',6'-trimethylphenyl)hexanoic acidHCID 12906146—
SolventSodium HydroxideHCID 14798—
Product2,3,5-Trimethyl-6-(5'-carboxy-1'-hydroxypentyl)-1,4-benzoquinoneHCID 12906157—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 6-hydroxy-6-(2'-hydroxy-3',4',6'-trimethylphenyl)hexanoic acid (formula II-3 wherein R=H3C, X=H, Y=OH, n=4, in the free form) (0.158 part) in 5% sodium hydroxide solution (2 volume parts) and water (7 volume parts) was added Fremy's salt (1 part) at room temperature with stirring. After being stirred for 1 hour, the mixture was cooled to 0° C., acidified with cold dilute hydrochloric acid, and extracted with ethyl acetate. The extract was washed with water, dried over anhydrous sodium sulfate, and concentrated in vacuo. The resulting residue was subjected to column chromatography on silica gel and eluted with chloroform-methanol (20:1). The product was recrystallized from ethylacetate-hexane (1:2) to give 2,3,5-trimethyl-6-(5'-carboxy-1'-hydroxypentyl)-1,4-benzoquinone (formula I-3 wherein R=H3C, n=4, in the free form) (0.128 part) as brown needles melting at 130°-131.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04407757
Source datasetuspto-grants-1983_10
ORD IDord-f49f5b0a582c402e80fe6291b02561d9
Source noteuspto-grants-1983_10