HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506304Generated: October 31, 2026
Bicarbonate Ion → 5-Phenyl-4-(trifluoromethyl)isoxazole-3-carbaldehyde
https://huagongshe.com/reaction/1506304
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bicarbonate Ion | HCID 769 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Triacetoxyperiodinane | HCID 159087 | — |
| Reactant | HCID 67168678 | HCID 67168678 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Phenyl-4-(trifluoromethyl)isoxazole-3-carbaldehyde | HCID 86669869 | 105.3% |
Reaction Steps
To a mixture of (5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)methanol (step A, 1.79 g, 7.36 mmol) in dichloromethane (23 mL) at 0° C. was added Dess-Martin Periodinane (3.43 g, 8.10 mmol). The reaction mixture was stirred at 0° C. for 10 min. and then at room temperature for 30 min. An additional 1.0 g of the Dess-Martin Periodinane was added, and the reaction mixture was stirred for an additional 30 min. A 1:1 mixture of saturated aqueous sodium thiosulfate and saturated aqueous bicarbonate (50 mL) was added slowly. The organic layer was collected, and the aqueous layer was extracted with dichloromethane (50 mL). The combined organic layers were dried over anhydrous sodium sulfate and concentrated under reduce pressure to give 5-phenyl-4-(trifluoromethyl)isoxazole-3-carbaldehyde (1.87 g, 7.75 mmol, quantitative yield) as a pale yellow oil. The compound had an HPLC ret. time=2.09 min. (condition A).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09216972B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-282bc2384a444b0c84a0f7abfc23669a |
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| Source note | uspto-grants-2015_12 |
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