HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695327Generated: November 1, 2026
Triphenylphosphine → HCID 66643884, compound
https://huagongshe.com/reaction/1695327
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | (5-Methyl-3-phenyl-1,2-oxazol-4-yl)methanol | HCID 2776149 | — |
| Reactant | 5-Hydroxy-1H-pyrazole-3-carboxylic acid methyl ester | HCID 178498602 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66643884 | HCID 66643884 | 27.9% |
Reaction Steps
To a stirred solution of 5-hydroxy-2H-pyrazole-3-carboxylic acid methyl ester (1.30 g, 9.15 mmol) and (5-methyl-3-phenyl-isoxazol-4-yl)-methanol (1.73 g, 9.15 mmol) in THF (80 mL) at 5° C. under argon was added triphenylphosphine (3.12 g, 11.9 mmol), then diethyl azodicarboxylate (2.07 g, 11.9 mmol) was added dropwise. The reaction mixture was warmed to room temperature and stirred overnight. The reaction mixture was then evaporated. Purification by chromatography (silica, heptane:ethyl acetate=1:1 then dichloromethane:methanol=9:1) gave a colorless oil (800 mg) which was triturated with diisopropylether and further purified using a 5×50 cm Chiralpak AD column at room temperature using an isopropanol:heptane (2:8) mobile phase with UV detection at 220 nM to afford the title compound (250 mg, 9%) as a white solid. MS: m/e=328.3 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163728B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-27ba284d6b304aacbbd8eb4a79295903 |
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| Source note | uspto-grants-2012_04 |
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