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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246422Generated: October 26, 2026

Triphenylphosphine → N-{4-[(Z)-2-(4-nitrophenyl)ethenyl]thiazol-2-yl}acetamide

https://huagongshe.com/reaction/1246422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant4-Nitrobenzyl bromideHCID 66011—
ReactantN-(4-Formyl-1,3-thiazol-2-YL)acetamideHCID 14931749—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
ProductN-{4-[(Z)-2-(4-nitrophenyl)ethenyl]thiazol-2-yl}acetamideHCID 5872025462.5%

Reaction Steps

1-(Bromomethyl)-4-nitrobenzene (1.9 g), triphenylphosphine (2.31 g) and N,N-dimethylformamide (20 ml) were combined under nitrogen atmosphere. The reaction mixture was stirred at room temperature for 2.5 hours. Then potassium tert-butoxide (1.19 g) and N-(4-formyl-1,3-thiazol-2-yl)acetamide (1.5 g) were added and the mixture was stirred at room temperature for 14 hours. The reaction mixture was poured into ice-water and extracted with ethyl acetate. The organic layer was washed with 1N-hydrochloric acid, water and saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated in vacuo. The residue was purified by flash column chromatography over silica gel with n-hexane/ethyl acetate (1:1)→(1:2) as an eluent, and triturated with ethyl ether to give N-{4-[(Z)-2-(4-nitrophenyl)ethenyl]-1,3-thiazol-2-yl}acetamide (1.59 g) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07125901B2
Source datasetuspto-grants-2006_10
ORD IDord-5a9019297d794bcab05cda333d414fd7
Source noteuspto-grants-2006_10