Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | benzothiazole, 2-nitro- | HCID 640709 | — |
| Reactant | HCID 70211764 | HCID 70211764 | — |
| Product | HCID 70212465 | HCID 70212465 | — |
Reaction Conditions
| Temperature | 232.5500030517578 °C |
|---|
Reaction Steps
A mixture of diethylfluorenyl benzothiazole, (9.0 g.), acetic acid (75 ml), and conc. nitric acid (sp. gr. 1.42, 25 ml) was held at 105° C. for 2 hours, cooled and filtered. These solids were stirred in dilute sodium hydroxide solution and filtered to get 10 g. of crude solid. This was recrystallized from toluene-heptane to afford 7.58 g., 75% of the nitrobenzothiazole, m.p. 209-2140C. Mass Spec: (m/z) 400(M+). Two recrystallizations from toluene-heptane raised the m.p. to 231.6-233.5° C. Anal. Calcd. for C24H20N2O2S: C, 71.98; H, 5.03; N, 7.00; S, 7.99. Found: C, 71.70, H, 4.90; N, 6.62; S, 7.77.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06300502B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-0f4a840795ac44aeb482a184e7aa2c69 |
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| Source note | uspto-grants-2001_10 |
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