HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039665Generated: November 1, 2026
Potassium Hydroxide → HCID 46846423, compound
https://huagongshe.com/reaction/2039665
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 46846424 | HCID 46846424 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 46846423 | HCID 46846423 | 98.4% |
Reaction Steps
To a slurry of ethyl 2-(4-(difluoromethoxy)-8-(methylsulfonamido)dibenzo[b,d]furan-1-yl)1,3-oxazole-4-carboxylate (0.2 g, 0.429 mmol) in ethanol (5 mL) and tetrahydrofuran (3 mL) was added potassium hydroxide (0.256 g, 4.562 mmol) in water (0.5 mL). Then it was stirred at room temperature for 16 hours. The solvent was removed in vacuum. The residue was diluted with water and acidified with 1N HCl until the solid separates out. The solid was filtered and washed with hexane. Yield—98.4%. 1H-NMR (DMSO-d6) δ: 3.09 (s, 3H), 7.40 (s, 1H), 7.48-7.51 (m, 1H), 7.59-7.63 (m, 2H), 7.87 (d, 1H), 8.06 (d, 1H), 8.97-8.99 (m, 2H), 9.81 (s, 1H); HPLC (purity): 99.1%; Mass calculated for C18K2F2N2O7S-438.4, observed—437.0; Rf—0.2 (Dichloromethane:Methanol (8:2)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08580795B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-57197807015547b39051ffc559dce5c8 |
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| Source note | uspto-grants-2013_11 |
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