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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734935Generated: October 25, 2026

Sodium Dithionite → 6-(10-Acetoxydecyl)-2,3-dimethoxy-5-methylhydroquinone

https://huagongshe.com/reaction/1734935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium DithioniteHCID 24489—
Reactant2-(10-(Acetyloxy)decyl)-5,6-dimethoxy-3-methyl-2,5-cyclohexadiene-1,4-dioneHCID 11090205—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product6-(10-Acetoxydecyl)-2,3-dimethoxy-5-methylhydroquinoneHCID 15294993—

Reaction Steps

2,3-Dimethoxy-6-(10-hydroxydecyl)-5-methyl-1,4-benzoquinone (3.38 g) was dissolved in dichloromethane (50 ml). Pyridine (1 ml) was added, and acetyl chloride (0.8 ml) was added with stirring under ice-cooling. After stirring for 1 hour at the same temperature, the mixture was washed with 0.1N hydrochloric acid (50 ml) followed by water (50 ml). The dichloromethane layer was concentrated under reduced pressure to obtain 6-(10-acetoxydecyl)-2,3-dimethoxy-5-methyl-1,4-benzoquinone as a red oil. This oil was dissolved in ether (50 ml), and a solution of sodium hydrosulfite (4 g) in water (50 ml) was added. Stirring was continued at room temperature until the red color of the ether layer disappeared. The ether layer was separated, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to obtain the desired compound (3.8 g) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05534639
Source datasetuspto-grants-1996_07
ORD IDord-98d1e31196eb48ee9a0b1737bd8f58b2
Source noteuspto-grants-1996_07