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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Boron tribromide methyl sulfide | HCID 10946916 | — |
| Reactant | 6-hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylic acid methyl ester | HCID 68700263 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 6-hydroxy-1-oxo-3-phenyl-1H-indene-2-carboxylic acid | HCID 68698982 | 48.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07745439B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-df3eb7c1c5c742609cdcc4e6d4b8dcbe |
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| Source note | uspto-grants-2010_06 |
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