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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374205Generated: October 28, 2026

Hydroquinone → HCID 178516562, compound

https://huagongshe.com/reaction/374205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroquinoneHCID 785—
ReactantSulfuric AcidHCID 1118—
ReactantSodium ChlorideHCID 5234—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178526187HCID 178526187—
SolventFormic AcidHCID 284—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
ProductHCID 178516562HCID 178516562—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred solution of 54.4 g. of 8-(2-furyl)-8-hydroxy-2-phenylthiooctanoic acid in 815 ml. of glyme and 610 ml. of water is added successively 0.5 g. of hydroquinone, 12.0 g. of sodium bicarbonate and 122 ml. of 90% formic acid. The resulting solution is heated at reflux temperature for 24 hours, cooled to 50° C. to produce a mixture of the 3-hydroxy and 4-hydroxy isomers. This is then treated dropwise with 40 ml. of concentrated sulfuric acid during 15 minutes. The resulting solution is refluxed for 18 hours, cooled, diluted with ethyl acetate and then saturated with sodium chloride. The organic layer is separated, washed with brine, dried and concentrated. The residue is subjected to chromatography on silica gel with chloroform progressively enriched in ether, giving 13.0 g. of the product as an oil, identified by its PMRδ 4.94 (1, broad s, CHOH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05166369
Source datasetuspto-grants-1992_11
ORD IDord-456665d3a6a54181928a724ead3b3cd1
Source noteuspto-grants-1992_11