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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656693Generated: October 30, 2026

Hydrochloric Acid → 4-(5-fluoro-2,3-dihydro-benzofuran-7-yl)-2-hydroxy-4-methyl-2-(trifluoromethyl)pentanoic Acid

https://huagongshe.com/reaction/656693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant5-Fluoro-2,3-dihydrobenzofuranHCID 22398640—
Reactant2-Hydroxy-4-methyl-2-(trifluoromethyl)pentenoic acidHCID 86624390—
SolventDichloromethaneHCID 6344—
Product4-(5-fluoro-2,3-dihydro-benzofuran-7-yl)-2-hydroxy-4-methyl-2-(trifluoromethyl)pentanoic AcidHCID 66726115—

Reaction Steps

A solution of 0.07 mol 5-fluoro-2,3-dihydro-benzofurane in 21 ml of dichloromethane is cooled to 3° C. To this solution 0.1 mol of AlCl3 is added over a period of 30 minutes. After this addition 0.05 mol of 2-hydroxy-4-methyl-2-(trifluoromethyl)pentenoic acid is added dropwise over 30 minutes. The mixture is stirred for at least 6 h under reflux conditions. After complete reaction the solution is poured on a mixture of ice (50 ml) and 1M HCl (10 ml) and stirred for at least 1 hour. The aqueous phase is extracted three times with 51 ml of ethylacetate. The combined organic phases are washed with water, saturated sodium chloride solution (brine) and dried over magnesiumsulfate. The solvent is evaporated under vacuum. The product may be recrystallized from n-heptane. As the title compound is yielded in highly pure form the recrystallization is not necessary. The title compound may be used directly to start the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071796B2
Source datasetuspto-grants-2011_12
ORD IDord-a9e207471b96415198fd408aa8f28bdd
Source noteuspto-grants-2011_12