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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646510Generated: October 30, 2026

Hydrochloric Acid → 4-Isobutylresorcinol

https://huagongshe.com/reaction/646510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantSodium HydroxideHCID 14798—
ReactantSodium borohydrideHCID 4311764—
Reactant1-(2,4-Dihydroxyphenyl)-2-methylpropan-1-oneHCID 15915731—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-IsobutylresorcinolHCID 13951085—

Reaction Steps

Ethyl chloroformate (3 eq) was added slowly to a cooled (0° C.) solution of 1-(2,4-dihydroxy-phenyl)-2-methyl-propan-1-one (1 eq) and triethylamine (3 eq) in THF. The mixture was warmed to ambient temperature and stirred for three hours before being filtered and the solids washed with cold THF. The combined filtrates were cooled to 0° C. and sodium borohydride (4 eq) in a volume of water equal to the THF filtrates added slowly. The mixture was warmed to ambient temperature, stirred for three hours and diluted with water. The mixture was twice extracted with diethyl ether, the combined extracts concentrated to dryness and re-suspended in 10% aqueous sodium hydroxide solution (4 eq). After refluxing for 90 minutes, the mixture was cooled, acidified with 5M aq HCl and twice extracted with diethyl ether. The organic extracts were dired over magnesium sulphate, filtered and concentrated to dryness to give 4-isobutyl-benzene-1,3-diol as a cloudy oil, which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07705027B2
Source datasetuspto-grants-2010_04
ORD IDord-2b8ee1447b5b40ecb241827a04d92efa
Source noteuspto-grants-2010_04