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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454827Generated: October 26, 2026

Triphenylphosphine → 2,2-dimethyl-N-[6-(4-trifluoromethyl-phenoxymethyl)-pyridin-2-yl]-propionamide

https://huagongshe.com/reaction/1454827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant4-(Trifluoromethyl)phenolHCID 67874—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantN-[6-(Hydroxymethyl)pyridin-2-yl]-2,2-dimethylpropanamideHCID 21782926—
SolventTolueneHCID 1140—
Product2,2-dimethyl-N-[6-(4-trifluoromethyl-phenoxymethyl)-pyridin-2-yl]-propionamideHCID 6884322492.8%

Reaction Steps

N-(6-Hydroxymethyl-pyridin-2-yl)-2,2-dimethyl-propionamide (0.625 g), triphenylphophine (0.786 g) and 4-trifluoromethyl-phenol (0.486 g) in toluene was treated at RT under an argon atmosphere with diisopropyl azodicarboxylate (0.67 g). The mixture was stirred for 2 h, partitioned between ice water and AcOEt, the layers were separated, the aqueous layer twice extracted with AcOEt. The combined organic layers were washed with water and saturated aqueous NaCl, dried over MgSO4, filtered and evaporated. The residue was purified by flash chromatography (heptane/AcOEt 100 to 85%) to give 2,2-dimethyl-N-[6-(4-trifluoromethyl-phenoxymethyl)-pyridin-2-yl]-propionamide (0.98 g) as a yellow oil. MS (ESI): 353.2 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482341B2
Source datasetuspto-grants-2009_01
ORD IDord-95b6212040154c8ea5f1448012f0e1a4
Source noteuspto-grants-2009_01