Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1679861Generated: November 2, 2026

Acetate → HCID 20277071, compound

https://huagongshe.com/reaction/1679861

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 2 N 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 numberUS04271083
Source datasetuspto-grants-1981_06
ORD IDord-aa2f9b1c862a483aa8a1f535a37edef1
Source noteuspto-grants-1981_06