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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53202Generated: October 29, 2026

Triphenylphosphine → HCID 19962069, compound

https://huagongshe.com/reaction/53202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactant3-(6-Chloropyridin-3-yl)propan-1-olHCID 14071569—
Reactant2,6-Dimethyl-4-(5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl)phenolHCID 135516666—
SolventDichloromethaneHCID 6344—
ProductHCID 19962069HCID 1996206978.3%

Reaction Steps

To a suspension of 1.12 g (4.34 mmol) of 4-(5-trifluoromethyl-1,2,4-oxadiazol-3-yl)-2,6-dimethylphenol, 0.87 g (1.2 eq) of 2-chloro-5-(3-hydroxypropyl)-pyridine, 1.4 g (1.2 eq) of triphenylphosphine in 50 ml of methylene chloride under nitrogen at 0° C. was added dropwise a solution of 0.86 g (1.2 eq) of DEAD in 5 ml of methylene chloride. The mixture was stirred under nitrogen at room temperature for 60 h, concentrated in vacuo and the residue was triturated with hexane/ethyl acetate, filtered, and the filtrate was concentrated in vacuo to yield a dark brown oil. The brown oil was purified by MPLC (50 id, Kieselgel 60 column, hexane/ethyl acetate, 3:1) to afford 1.4 g (78%) of 2-chloro-5-[3-[4-(5-trifluoromethyl-1,2,4-oxadiazol-3-yl)-2,6-dimethylphenoxy]-propyl]-pyridine, as a white crystalline solid, m.p. 89°-91° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05618821
Source datasetuspto-grants-1997_04
ORD IDord-11e67ddc3a724fc5b0de43993bbd3718
Source noteuspto-grants-1997_04