HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441560Generated: October 30, 2026
Hydrochloric Acid → 3-(3-bromophenyl)-N-ethylprop-2-enamide
https://huagongshe.com/reaction/441560
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | Ethyl 3-(3-bromophenyl)acrylate | HCID 5369361 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(3-bromophenyl)-N-ethylprop-2-enamide | HCID 42754 | — |
Reaction Steps
Trans ethyl 3-bromocinnamate (8.4 g), ethylamine (6.7 g), methanol (18 ml) and 4A molecular sieves (1 g) were combined and heated at reflux for 1/2 hour. The mixture was cooled to about 45° C. and sodium methylate (0.6 g) added. The mixture was then heated at reflux 11/2 hour and then cooled. It was acidified with concentrated hydrochloric acid (12 ml). The sieves were removed by filtration. Ice water was added to the filtrate to precipitate trans 3-bromo-N-ethylcinnamamide, m.p. 89°-90° C. (after recrystallization from ethanol/water).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04041071 |
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| Source dataset | uspto-grants-1977_08 |
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| ORD ID | ord-ce7df936a4914e7a9cceb8701663e7c0 |
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| Source note | uspto-grants-1977_08 |
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