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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1679862Generated: October 30, 2026

HCID 20277060, compound → HCID 20277073, compound

https://huagongshe.com/reaction/1679862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 20277060HCID 20277060—
SolventDiethyl EtherHCID 3283—
ProductHCID 20277073HCID 20277073—

Reaction Steps

A solution of 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) (0.1 part) in diethyl ether (10 volume parts) was stirred with 3% aqueous ferric chloride solution at room temperature for 2 hours. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The combined organic layer and diethyl ether extract were washed with water, dried over anhydrous sodium sulfate, and evaporated in vacuo to dryness. The residue was subjected to chromatography on silica gel and eluted with diethyl ether to give 2,3,5-trimethyl-6-(6'-hydroxy-1'-oxohexyl)-1,4-benzoquinone (formula IV-1 wherein R=H3C, n=4, in the free form) (0.088 part) as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04271083
Source datasetuspto-grants-1981_06
ORD IDord-4930128e978e4337abac7a8e157f93e8
Source noteuspto-grants-1981_06