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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248605Generated: November 3, 2026

Acetate → HCID 20277071, compound

https://huagongshe.com/reaction/1248605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetateHCID 175—
ReactantSodium HydroxideHCID 14798—
ReactantSodium DithioniteHCID 24489—
ReactantHCID 12906159HCID 12906159—
SolventMethanolHCID 887—
ProductHCID 20277071HCID 20277071—

Reaction Steps

To a stirred mixture of 2,3,5-trimethyl-6-(6'-acetoxy-1'-oxohexyl)-1,4-benzoquinone (formula IV-1 wherein R=H3C, n=4, in the form of acetate) (0.5 part), sodium hydrosulfite (1 part) and 30% aqueous methanol (20 volume parts) was added dropwise 2N aqueous sodium hydroxide (1.6 volume part) at 5° C. The mixture was allowed to stand for 3 hours at the same temperature. After removal of the methanol and acidification with phosphoric acid, the product was extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous sodium sulfate, and evaporated in vacuo. The residue was subjected to chromatography on silica gel and eluted with ethyl acetate to give 2,3,5-trimethyl-6-(6'-acetoxy-1'-oxohexyl)hydroquinone. (formula III-1 wherein R=H3C, X=Y=OH, n=4, in the form of acetate) (0.075 part). Further elution with the same solvent gave 2,3,5-trimethyl-6-(6'-hydroxy-1'-oxohexyl)-hydroquinone. (formula III-1 wherein R=H3C, X=Y=OH, n=4, in the free form) (0.265 part).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04525361
Source datasetuspto-grants-1985_06
ORD IDord-a88bdd1f88134d0cbc62aaf135850e82
Source noteuspto-grants-1985_06