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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245338Generated: October 25, 2026

Potassium Carbonate → 6-(4-{[Tert-butyl(dimethyl)silyl]oxy}butyl)-7-propyl-3-(trifluoromethyl)-1,2-benzisoxazole

https://huagongshe.com/reaction/1245338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant9-Borabicyclo(3.3.1)nonaneHCID 78966—
Reactant(But-3-enyloxy)(tert-butyl)dimethylsilaneHCID 10008065—
Reactant7-Propyl-3-(trifluoromethyl)-1,2-benzisoxazol-6-yl trifluoromethanesulfonateHCID 21910991—
CatalystPalladiumHCID 23938—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product6-(4-{[Tert-butyl(dimethyl)silyl]oxy}butyl)-7-propyl-3-(trifluoromethyl)-1,2-benzisoxazoleHCID 21911017—

Reaction Steps

To a solution of (but-3-enyloxy)(tert-butyl)dimethylsilane, from this Example step 2, (148 mg, 0.79 mmol) in dry THF (0.25 mL) was added 9-BBN (0.5M 1.75 mL, 0.88 mmol) at 0° C. under N2. The mixture was stirred for 5 hours, then added to a mixture of 7-propyl-3-(trifluoromethyl)-1,2-benzisoxazol-6-yl trifluoromethanesulfonate, as prepared in this Example step 1, (300 mg, 0.79 mmol), K2CO3 (220 mg, 1.59 mmol), and dichlorobis(triphenylphosphene) palladium (32.5 mg, 0.039 mmol) in DMF (3 mL) under N2 in a sealed tube. The mixture was stirred overnight at 55° C. The reaction mixture was partitioned between ethyl acetate and water. Combined organic extracts were washed with water twice and brine and then dried over Na2SO4. The solvent was evaporated in vacuo. The residue was purified by chromatography on silica gel using ethyl acetate and hexane (1:30) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07125865B2
Source datasetuspto-grants-2006_10
ORD IDord-0a561ba0647e46139d81dab0bac9f51b
Source noteuspto-grants-2006_10