HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246426Generated: October 31, 2026
Triphenylphosphine → HCID 21914748, compound
https://huagongshe.com/reaction/1246426
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 4-Nitrobenzyl bromide | HCID 66011 | — |
| Reactant | N-(4-Formyl-1,3-thiazol-2-YL)acetamide | HCID 14931749 | — |
| Reactant | Potassium butoxide | HCID 23699084 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 21914748 | HCID 21914748 | 91.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07125901B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-127011b10c5446a4be72a0a2f68d4fda |
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| Source note | uspto-grants-2006_10 |
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