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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248604Generated: October 30, 2026

Acetate → HCID 12906159, compound

https://huagongshe.com/reaction/1248604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetateHCID 175—
ReactantDiethyl EtherHCID 3283—
ReactantHCID 20277068HCID 20277068—
ReactantJones' reagentHCID 131709961—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
ProductHCID 12906159HCID 12906159—

Reaction Steps

A solution of 2,3,5-trimethyl-6-(6'-acetoxy-1'-hydroxyhexyl)-1,4-benzoquinone (formula IV-3 wherein R=H3C, n=4, in the form of acetate at --CH2OH) (0.74 part) in acetone (20 volume parts) was oxidized at 5° C. for 5 minutes with Jones reagent (0.6 volume part) prepared by dissolving chromic trioxide (26.72 parts) in concentrated sulfuric acid (23 volume parts) diluted with water to a volume of 100 volume parts. The resulting precipitate was decomposed with water, and the product was taken up with diethyl ether. The organic layer was washed with water and dried over anhydrous sodium sulfate. The residue upon removal of the solvent was subjected to column chromatography on silica gel and eluted with methylene chloride and the resulting product was crystallized from petroleum ether to give 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) (0.638 part) as yellow crystals melting at 57° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04525361
Source datasetuspto-grants-1985_06
ORD IDord-3247676b6c2f4c24a57bae5a646c6501
Source noteuspto-grants-1985_06