HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171707Generated: October 31, 2026
Triphenylphosphine → HCID 68310297, compound
https://huagongshe.com/reaction/2171707
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Benzyl 3-hydroxyazetidine-1-carboxylate | HCID 10081755 | — |
| Reactant | HCID 72222662 | HCID 72222662 | — |
| Reactant | HCID 178459888 | HCID 178459888 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68310297 | HCID 68310297 | 29.8% |
Reaction Steps
Benzyl 3-hydroxyazetidine-1-carboxylate (2.3 g) and 6-tert-butoxypyridin-3-ol (1.5 g) were mixed with THF (25 ml), and triphenylphosphine (4 g) was added thereto. A 1.9 M DIAD/toluene solution (8 ml) was added dropwise thereto, followed by stirring at 55° C. overnight. The reaction mixture was concentrated under reduced pressure. The obtained residue was mixed with ethanol (25 ml), and 10% palladium carbon (800 mg) were added thereto, followed by stirring at room temperature for 5 hours under hydrogen atmosphere. The reaction mixture was filtered using Celite as a filtration adjuvant, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (CHCl3/MeOH) to obtain 5-(azetidin-3-yloxy)-2-tert-butoxypyridine (595 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051283B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-f358b2c47fbe40359d47cdbcfea818c7 |
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| Source note | uspto-grants-2015_06 |
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