HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117832Generated: October 26, 2026
Triphenylphosphine → N-{4-[(Z)-2-(4-nitrophenyl)ethenyl]thiazol-2-yl}acetamide
https://huagongshe.com/reaction/2117832
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 4-Nitrobenzyl bromide | HCID 66011 | — |
| Reactant | N-(4-Formyl-1,3-thiazol-2-YL)acetamide | HCID 14931749 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-{4-[(Z)-2-(4-nitrophenyl)ethenyl]thiazol-2-yl}acetamide | HCID 58720254 | 62.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07442715B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-4065306d42d34d8e9b6d49e028139f96 |
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| Source note | uspto-grants-2008_10 |
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