Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Aminobenzonitrile | HCID 13396 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 23501186 | HCID 23501186 | 64.4% |
Reaction Steps
2,4,6-trichloro-1,3,5-triazine (0.07440 mol) and tetrahydrofuran (100 ml) were combined and cooled to −75° C. under Ar atmosphere. 4-Aminobenzonitrile (0.07440 mol) was added and the solution was stirred for 4 hours at −75° C. Triethylamine (0.07440 mol) was added dropwise and the reaction mixture was allowed to warm up slowly to room temperature and stirred for 3 days. After adding 1,4-dioxane (100 ml), the resulting precipitate was collected by filtration, washed with tetrahydrofuran, and dried, yielding 12.74 g 4-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]benzonitrile (interm. 17).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07887845B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-b12f79ba896a412c9f85a871a4d4b6d9 |
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| Source note | uspto-grants-2011_02 |
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