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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021296Generated: October 31, 2026

Trifluoroacetic acid → HCID 71777794, compound

https://huagongshe.com/reaction/1021296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriphenylphosphineHCID 11776—
Reactant2-Methyl-5-hydroxypyridineHCID 14275—
ReactantTert-butyl 3-hydroxyazetidine-1-carboxylateHCID 2756801—
ReactantHCID 178459888HCID 178459888—
Solvent1,2-DichloroethaneHCID 11—
SolventTetrahydrofuranHCID 8028—
ProductHCID 71777794HCID 7177779431.4%

Reaction Conditions

Temperature55 °C

Reaction Steps

tert-Butyl 3-hydroxyazetidine-1-carboxylate (1.0 g) and 6-methylpyridin-3-ol (570 mg) were mixed with THF (10 ml), and triphenylphosphine (2.3 g) was added thereto. A 1.9 M DIAD/toluene solution (4.5 ml) was added dropwise thereto, followed by stirring at 55° C. overnight. The reaction mixture was concentrated under reduced pressure, and EtOAc and 1 M hydrochloric acid were added thereto. The aqueous layer was adjusted to pH of around 10 by the addition of a 4 M aqueous NaOH solution, followed by extraction with CHCl3. The organic layer was dried over Na2SO4 and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (CHCl3/MeOH). The purified product thus obtained was mixed with DCE (6 ml), and TFA (3 ml) was added thereto, followed by stirring at room temperature for 5 hours. The reaction mixture was concentrated under reduced pressure, and then CHCl3 and a 1 M aqueous NaOH solution were added thereto. The organic layer was dried over Na2SO4 and then concentrated under reduced pressure to obtain 5-(azetidin-3-yloxy)-2-methylpyridine (269 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716470B2
Source datasetuspto-grants-2014_05
ORD IDord-ef238fc593184994b0105586810bfcca
Source noteuspto-grants-2014_05