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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 5-Fluoro-2,3-dihydrobenzofuran | HCID 22398640 | — |
| Reactant | 2-Hydroxy-4-methyl-2-(trifluoromethyl)pentenoic acid | HCID 86624390 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(5-fluoro-2,3-dihydro-benzofuran-7-yl)-2-hydroxy-4-methyl-2-(trifluoromethyl)pentanoic Acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071796B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-a9e207471b96415198fd408aa8f28bdd |
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| Source note | uspto-grants-2011_12 |
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