Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl 3-(N,N-dimethylamino)acrylate | HCID 121015 | — |
| Reactant | 4-Bromo-2-chlorobenzoyl chloride | HCID 15592207 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 54513699 | HCID 54513699 | 68% |
Reaction Steps
30.2 g of ethyl 3-dimethylaminoacrylate and 29.3 ml of triethylamine are dissolved in 180 ml of toluene and boiled at reflux. At this temperature a solution of 53 g of 4-bromo-2-chloro-benzoyl chloride (U.S. Pat. No. 4,959,363) in 50 ml of toluene is added dropwise over 30 min. and the mixture is subsequently heated at reflux for a further 1 hr. The mixture is left to cool to room temperature and is stirred in an ice bath for a further 30 min. The suspension is filtered and the precipitated triethylamine hydrochloride is washed with 40 ml of ice-cold toluene. The filtrate is concentrated to half of its volume and then, for crystallization, diluted with 100 ml of hexane and stirred in an ice bath for 1 hr. 51.2 g (67%) of ethyl 2-(4-bromo-2-chloro-benzoyl)-3-dimethylaminoacrylate are obtained as colourless crystals. M.p. 100°-101°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05763450 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-085fa8c5d0844df5aa5c49e9f398eaa7 |
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| Source note | uspto-grants-1998_06 |
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