HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35901Generated: October 28, 2026
Dimethylformamide → HCID 19939348, compound
https://huagongshe.com/reaction/35901
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 19939340 | HCID 19939340 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 19939348 | HCID 19939348 | 90% |
Reaction Steps
A mixture of 1.00 g (3.77 mmol)3 -(4-carboxyphenyl)-N-phenylpropiolamide, 1.00 g (excess) anhydrous sodium bicarbonate and 25 mL dry N,N-dimethylformamide was stirred at room temperature. Added was 1.95 g (excess) iodoethane and the mixture heated at 70°-80° C. for 3 hrs. The mixture was allowed to cool to room temperature and poured into 75 mL water. The resulting solid was filtered and recrystallized from ethanol/water to provide 0.99 g (3.37 mmol, 90%)3-(4-carbethoxyphenyl)-N-phenylpropiolamide as a pale, yellow powder, mp=114°-115° C. NMR (CDCl3 /TMS): 1.40 (t, 3H), 4.39 (q, 2H), 7.16 (t, 1H), 7.36 (t, 2H), 7.60 (d, 4H), 7.90 (s, 1H), 8.03 (d, 2H)). IR (KBr): 3292, 2210, 1692, 1660. High resolution mass spectrum: Calculated; 294.113019. Measured; 294.112376.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05411977 |
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| Source dataset | uspto-grants-1995_05 |
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| ORD ID | ord-caa5fbc3b70d4daf8b055a25bf133994 |
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| Source note | uspto-grants-1995_05 |
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