HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 332352Generated: October 26, 2026
Triphenylphosphine → 6-(3-Phenyl-5-trifluoromethyl-isoxazol-4-ylmethoxy)-nicotinic acid methyl ester
https://huagongshe.com/reaction/332352
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | (3-Phenyl-5-(trifluoromethyl)isoxazol-4-yl)methanol | HCID 57732616 | — |
| Reactant | HCID 178498304 | HCID 178498304 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-(3-Phenyl-5-trifluoromethyl-isoxazol-4-ylmethoxy)-nicotinic acid methyl ester | HCID 68443269 | 42.6% |
Reaction Steps
To a solution of (3-phenyl-5-trifluoromethyl-isoxazol-4-yl)-methanol (100 mg, 0.41 mmol) in THF (5 mL) was added 6-hydroxy-nicotinic acid methyl ester (69.3 mg, 0.45 mmol) and triphenylphosphine (162 mg, 0.62 mmol) at ambient temperature under an argon atmosphere. Then diethyl azodicarboxylate (96 μL, 0.62 mmol) was added and the reaction mixture was heated at 50° C. for 2 h. After cooling to room temperature the mixture was evaporated. Purification by chromatography (SiO2, heptane:ethyl acetate=100:0 to 1:1) afforded the title compound (66 mg, 42%) as all off-whit solid. MS: m/e=379.5 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877783B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-0d4efff7064f47fd83ad12139c46b164 |
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| Source note | uspto-grants-2014_11 |
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