Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBicarbonate IonHCID 769—
ReactantSodium ThiosulfateHCID 24477—
ReactantTriacetoxyperiodinaneHCID 159087—
ReactantHCID 67168678HCID 67168678—
SolventDichloromethaneHCID 6344—
Product5-Phenyl-4-(trifluoromethyl)isoxazole-3-carbaldehydeHCID 86669869105.3%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216972B2
Source datasetuspto-grants-2015_12
ORD IDord-282bc2384a444b0c84a0f7abfc23669a
Source noteuspto-grants-2015_12