HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1450195Generated: October 27, 2026
Sodium Hydroxide → 5-Fluoro-2-(4-fluorophenyl)-2,3-dihydro-2-hydroxy-1H-inden-1-one
https://huagongshe.com/reaction/1450195
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Triethyl phosphite | HCID 31215 | — |
| Reactant | 5-fluoro-2-(4-fluorophenyl)-2,3-dihydro-1H-inden-1-one | HCID 19975435 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-Fluoro-2-(4-fluorophenyl)-2,3-dihydro-2-hydroxy-1H-inden-1-one | HCID 19975432 | 38.8% |
Reaction Steps
A solution of 7.0 g (0.029 moles) of the product obtained from Step A and 69 mL of toluene was added with stirring to a mixture of 5.7 g (0.034 moles) of triethylphosphite, 0.33 g (0.0014 moles) of benzyltriethylammonium chloride, 344 mL of toluene and 167 mL of 50% aqueous sodium hydroxide solution. A steady stream of air was introduced into the vigorously stirred reaction mixture at room temperature for I hour. The resulting mixture was partitioned between hexane/ether and water and the aqueous layer was extracted three times with ether. The combined organic layers were washed twice with water, three times with saturated aqueous sodium bisulfite solution, dried over magnesium sulfate and concentrated. The resulting crude product was triturated several times with hexanes to afford 2.93 g of a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05602126 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-4bd5a0aa855c46698a5244397025273e |
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| Source note | uspto-grants-1997_02 |
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