Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | HCID 67753963 | HCID 67753963 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 85317206 | HCID 85317206 | 69% |
Reaction Steps
A solution of p-chloro-β-(methylamino)cinnamonitrile (19.3 g, 0.1 mol) in carbon tetrachloride at 70° C. is treated dropwise with a solution of bromine (16.8 g, 0.105 mol) in carbon tetrachloride over a 30-40 minute period (tetrahydrofuran is added as needed during the bromine addition to aid dissolution of the reaction mixture). The reaction mixture is stirred for 30 minutes at 70° C., cooled to room temperature and concentrated to give a yellow crystalline precipitate. The mixture is filtered, the filter cake is washed with carbon tetrachloride and dried to give the title product as a yellow solid, 18.8 g (69% yield), mp 178.0°-178.5° C., identified by IR, NMR and mass spectral analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05256796 |
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| Source dataset | uspto-grants-1993_10 |
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| ORD ID | ord-1011f82c72434ea684181eb3fe02a6e7 |
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| Source note | uspto-grants-1993_10 |
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