HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277182Generated: October 31, 2026
Triphenylphosphine → HCID 86731239, compound
https://huagongshe.com/reaction/2277182
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1,1-Dimethylethyl N-((1S)-2-hydroxy-1-methylethyl)carbamate | HCID 7023103 | — |
| Reactant | Hydrogen chloride-ethyl acetate | HCID 21866389 | — |
| Reactant | DIAD toluene | HCID 66880968 | — |
| Reactant | HCID 86731237 | HCID 86731237 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86731239 | HCID 86731239 | 53.9% |
Reaction Steps
To a solution of 2-(4-(cyclopropylmethoxy)-3-fluorophenyl)-7-fluoro-1,3-benzoxazol-6-ol (3.96 g), tert-butyl ((2S)-1-hydroxypropan-2-yl)carbamate (3.28 g) and triphenylphosphine (4.91 g) in THF (50 mL) was added dropwise diisopropyl azodicarboxylate toluene solution (1.9 M, 9.85 mL) at 0° C., and the mixture was stirred at room temperature for 30 min. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (NH, hexane/ethyl acetate) to give a solid. To this solid was added 4 M hydrogen chloride/ethyl acetate (50 mL), and the mixture was stirred at room temperature for 10 min, and concentrated. To the residue were added pyridine (50 mL) and acetic anhydride (50 mL), and the mixture was stirred at room temperature for 15 min. The reaction mixture was concentrated under reduced pressure, and the obtained solid was dissolved in ethyl acetate/methanol, and the solution was subjected to silica gel column chromatography (NH, ethyl acetate), and concentrated. The obtained solid was recrystallized (hexane/ethyl acetate) to give the title compound as white crystals (2.80 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09133129B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-4a6e170bef584ad8b7b294d64156625a |
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| Source note | uspto-grants-2015_09 |
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