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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77112Generated: October 29, 2026

Trisodium Phosphate → 1236188-80-9

https://huagongshe.com/reaction/77112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrisodium PhosphateHCID 24243—
ReactantSodium SulfiteHCID 24437—
ReactantSodium ChloriteHCID 23668197—
Reactant(3-Phenyl-4-(trifluoromethyl)isoxazol-5-yl)methanolHCID 66955108—
CatalystTempoHCID 2724126—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product1236188-80-9HCID 5837409499%

Reaction Conditions

Temperature35 °C

Reaction Steps

A mixture of (3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)methanol (2.1 g, 8.64 mmol), TEMPO (0.094 g, 0.604 mmol), and a sodium phosphate buffer (0.67M) (32.2 mL, 21.59 mmol) in acetonitrile (30 mL) was heated to 35° C. A fresh solution of sodium phosphate buffer (40 mL, pH ˜6.5) consisting of a 1:1 solution of NaH2PO4 (20 mL, 0.67M) and Na2HPO4 (20 mL, 0.67M) was prepared and used. Solutions of sodium chlorite (3.91 g, 34.5 mmol) in water (4.5 mL) and bleach (4.3 mL, 6% wt.) were added simultaneously over 40 min. The reaction was monitored by HPLC, and after 2 h, ˜30% of the starting material remained. After 6 h, 10% remained. Additional bleach (100 μL) was added, and the reaction mixture was left at room temperature overnight. Additional bleach (100 μL) was added. The resulting mixture was allowed to stir at 35° C. for additional 2 h. HPLC indicated complete conversion. The reaction was quenched by the slow addition of a solution of sodium sulfite (2.07 mL, 43.2 mmol) in water (90 mL) at 0° C., resulting in the disappearance of the brown reaction color. The solvent was removed under reduced pressure, and the remaining aqueous residue was extracted with ethyl acetate (3×40 mL). The organic layers were combined, washed with water (8 mL), washed with brine (8 mL), and dried over anhydrous sodium sulfate. Concentration under reduced pressure afforded 3-phenyl-4-(trifluoromethyl)isoxazole-5-carboxylic acid (2.2 g, 8.55 mmol, 99% yield) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835470B2
Source datasetuspto-grants-2014_09
ORD IDord-3517342d88fc4f399422327644a26e83
Source noteuspto-grants-2014_09