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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19554Generated: October 25, 2026

Hydrochloric Acid → 6-hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylic acid

https://huagongshe.com/reaction/19554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
ReactantBoron tribromide methyl sulfideHCID 10946916—
Reactant6-hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylic acid methyl esterHCID 68700263—
Solvent1,1-DichloroethaneHCID 6365—
Product6-hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylic acidHCID 6869898248.6%

Reaction Conditions

Temperature90 °C

Reaction Steps

6-Hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylic acid methyl ester (2.6 g, 9.28 mmol) obtained in Step 1 was dissolved in dichloroethane, and boron tribromide methyl sulfide (6.0 mL, 27.84 mmol) was added thereto. The mixture was refluxed for 2 hrs at 90° C., cooled in an ice bath, neutralized using sodium bicarbonate, and adjusted to pH 2 using 6N hydrochloric acid. The resulting mixture washed successively with dichloromethane and water. The organic layer was separated, dried over anhydrous MgSO4, concentrated under a reduced pressure and recrystallized to obtain 1.2 g of the titled compound (yield: 48.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745439B2
Source datasetuspto-grants-2010_06
ORD IDord-df3eb7c1c5c742609cdcc4e6d4b8dcbe
Source noteuspto-grants-2010_06