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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534853Generated: October 30, 2026

Dimethylformamide → Methyl 3-(4-(3-cyano-5-(trifluoromethyl)phenyl)-oxazol-2-yl)propanoate

https://huagongshe.com/reaction/534853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantMethyl 3-(4-(3-bromo-5-(trifluoromethyl)phenyl)oxazol-2-yl)propanoateHCID 66750877—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
CatalystHCID 178418397HCID 178418397—
SolventEthyl AcetateHCID 8857—
ProductMethyl 3-(4-(3-cyano-5-(trifluoromethyl)phenyl)-oxazol-2-yl)propanoateHCID 6675130775%

Reaction Conditions

Temperature100 °C

Reaction Steps

A suspension of methyl 3-(4-(3-bromo-5-(trifluoromethyl)phenyl)oxazol-2-yl)-propanoate (Reference Example 44, 0.645 g, 1.71 mmol) and zinc cyanide (0.120 g, 1.02 mmol) in DMF (15.0 mL) was evacuated and purged with nitrogen. To this reaction mixture was added tetrakis(triphenylphosphine)palladium(0) (0.197 g, 0.170 mmol) and the resulting reaction mixture was heated at 100° C. for 8 h. After this time, the reaction mixture was cooled to room temperature, diluted with ethyl acetate, washed with water and saturated sodium chloride, dried (Na2SO4), filtered and concentrated under reduced pressure. The resulting residue was purified by flash column chromatography (silica gel, hexanes/ethyl acetate 4:1) to provide methyl 3-(4-(3-cyano-5-(trifluoromethyl)phenyl)-oxazol-2-yl)propanoate (0.417 g, 75%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853215B2
Source datasetuspto-grants-2014_10
ORD IDord-5f8b38ad77e6442ba5e32e506dab163e
Source noteuspto-grants-2014_10