Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzamide | HCID 2331 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | (Z)-1,4-dibromobut-2-ene | HCID 5354994 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1H-Pyrrole, 1-benzoyl-2,5-dihydro- | HCID 11252283 | — |
Reaction Steps
121 g (1 mol) of benzamide in 3 l of toluene are introduced initially, 200 g of powdered potassium hydroxide are introduced with stirring, 32 g (0.1 mol) of tetrabutylammonium bromide are added and the mixture is heated to 40° C. 243 g (1 mol) of 88% cis-1,4-dibromo-2-butene are then added dropwise in such a way that the internal temperature does not exceed 60° C. The mixture is stirred for another 5 hours at 50° C., then poured into water, and the organic phase is separated off, washed with water, dried and concentrated. The residue is distilled under reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05436334 |
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| Source dataset | uspto-grants-1995_07 |
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| ORD ID | ord-6ef41715b4a041a9bc6dc8d77e639fe4 |
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| Source note | uspto-grants-1995_07 |
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