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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117836Generated: November 2, 2026

Triphenylphosphine → HCID 21914748, compound

https://huagongshe.com/reaction/2117836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant4-Nitrobenzyl bromideHCID 66011—
ReactantN-(4-Formyl-1,3-thiazol-2-YL)acetamideHCID 14931749—
ReactantPotassium butoxideHCID 23699084—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 21914748HCID 2191474891.8%

Reaction Steps

A mixture of 4-nitrobenzyl bromide (6.35 g), triphenylphosphine (7.71 g) and N,N-dimethylformamide (50 ml) was stirred for 5 hours at room temperature. To the mixture were added potassium butoxide (3.96 g), and then N-(4-formyl-1,3-thiazol-2-yl)acetamide (5.0 g) prepared in a similar manner according to Step 4 of Production Example 1, and the mixture was stirred for 13 hours at the same temperature. The reaction mixture was poured into ethyl acetate (200 ml) and water (200 ml). The organic layer was washed with water (20 ml), dried over sodium sulfate and concentrated in vacuo. The crystalline residue was collected and washed with 30% ethyl acetate/diisopropyl ether to give N-{4-[(E)-2-(4-nitrophenyl)ethenyl]-1,3-thiazol-2-yl}acetamide (7.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442715B2
Source datasetuspto-grants-2008_10
ORD IDord-64b5e79c2df6471fac2f6dea5a3215a4
Source noteuspto-grants-2008_10