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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 9-Borabicyclo(3.3.1)nonane | HCID 78966 | — |
| Reactant | (But-3-enyloxy)(tert-butyl)dimethylsilane | HCID 10008065 | — |
| Reactant | 7-Propyl-3-(trifluoromethyl)-1,2-benzisoxazol-6-yl trifluoromethanesulfonate | HCID 21910991 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-(4-{[Tert-butyl(dimethyl)silyl]oxy}butyl)-7-propyl-3-(trifluoromethyl)-1,2-benzisoxazole | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07125865B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-0a561ba0647e46139d81dab0bac9f51b |
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| Source note | uspto-grants-2006_10 |
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