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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021307Generated: November 3, 2026

Triphenylphosphine → HCID 68310297, compound

https://huagongshe.com/reaction/1021307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantBenzyl 3-hydroxyazetidine-1-carboxylateHCID 10081755—
ReactantHCID 72222662HCID 72222662—
ReactantHCID 178459888HCID 178459888—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68310297HCID 6831029729.8%

Reaction Conditions

Temperature55 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716470B2
Source datasetuspto-grants-2014_05
ORD IDord-afa0ff41d2c74245bde7a56f68a30f07
Source noteuspto-grants-2014_05