Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | O-Phenylenediamine | HCID 7243 | — |
| Reactant | Methyl nitrite | HCID 12231 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178418385 | HCID 178418385 | — |
Reaction Steps
108 g of freshly distilled 99.8% pure o-phenylenediamine were suspended in 125 ml of methanol and heated to 50° C. At this temperature, gaseous methyl nitrite, prepared from sodium nitrite solution (25% strength), methanol and sulphuric acid (48% strength), was introduced. The rate of addition was such that no off-gas left the reaction flask. As soon as the reaction mixture did not absorb any more gas (about 2 hours), a sample was removed and tested for complete conversion. This was followed by first distilling off methanol and then water from the reaction mixture. With the addition of polywax (polydiol 1550) as a lubricant, the mixture was then distilled continuously through a thin-film evaporator at 4 mbar and a heater temperature of 220° C. Benzotriazole came over at about 165° C. and 4 mbar. Such freshly distilled benzotriazole is 99.9% pure, as analyzed by gas chromatography. It has a slightly yellow colour. On standing for several weeks, the pale yellow colour fades to a palate beige colour.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04918195 |
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| Source dataset | uspto-grants-1990_04 |
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| ORD ID | ord-ea6eb17e3c254644af4443b7bba2a062 |
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| Source note | uspto-grants-1990_04 |
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