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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749104Generated: October 30, 2026

Hydrochloric Acid → 4,5,6,7-Tetrahydro-3-hydroxy-1(3H)-isobenzofuranone

https://huagongshe.com/reaction/749104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3,4,5,6-Tetrahydrophthalic anhydrideHCID 12475—
ReactantSodium borohydrideHCID 4311764—
SolventTetrahydrofuranHCID 8028—
Product4,5,6,7-Tetrahydro-3-hydroxy-1(3H)-isobenzofuranoneHCID 1090977753.3%

Reaction Steps

To a solution of 3,4,5,6-tetrahydrophthalic acid anhydride (10.0 g) in tetrahydrofuran (50.0 mL) was added sodium borohydride (600 mg) in ice bath. The mixture was stirred at room temperature for 30 minutes and refluxed for 5 hours. After cooling to room temperature, 1N hydrochloric acid (10.0 mL) was added to the reaction mixture, which was concentrated. Water was added to the residue, which was extracted with ethyl acetate. The extract was washed with water and brine sequentially, dried over anhydrous magnesium sulfate and concentrated. The residue was purified by column chromatography on silica gel (ethyl acetate:hexane=1:4) to give the title compound (5.40 g) having the following physical data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07402580B2
Source datasetuspto-grants-2008_07
ORD IDord-7292adb0b1aa4923b80c84e5b99ceb74
Source noteuspto-grants-2008_07