Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | O-Phenylenediamine | HCID 7243 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Selenium | HCID 6326970 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Benzimidazol-2-one | HCID 162542 | 99% |
Reaction Steps
o-Phenylenediamine 1.35 g (12.5 m moles), selenium powder 0.99 g (12.5 m moles), water 1.6 ml (89 m moles), triethylamine 5 g (50 m moles) and tetrahydrofuran 100 ml were placed in a 200-ml capacity autoclave, and the atmosphere therein was replaced by carbon monoxide of 20 Kg/cm2. The contents in the autoclave were heated to 80° C. and held at the temperature for 3 hours with stirring. Thereafter the reaction mixture was cooled to room temperature, and carbon monoxide was removed from the autoclave. The reaction mixture was taken out of the autoclave and worked up in the same manner as in EXAMPLE 1 to provide benzimidazolone 1.66 g (99.0% yield) of 95.6% purity.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04374250 |
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| Source dataset | uspto-grants-1983_02 |
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| ORD ID | ord-4b0cfb6db46646239f2f4f823b9c2065 |
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| Source note | uspto-grants-1983_02 |
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