Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | HCID 14033195 | HCID 14033195 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | HCID 13960985 | HCID 13960985 | 89.6% |
Reaction Steps
6-Fluoro-3-(1-methylethyl)-2-(3H)-benzothiazolone (299 g) was dissolved in concentrated sulfuric acid (8750 g), and the resultant mixture was cooled to a temperature of -5° to 0° C. 98% fuming nitric acid (d=1.52) (94.68 g) was dropwise added thereto while maintaining the temperature at 0° C., followed by stirring for 1 hour. The reaction mixture was poured into ice-water (16 kg), and the precipitated crystals were collected by filtration. Crystals were washed with water and dried to give 325 g of 6-fluoro-3-(1-methylethyl)-5-nitro-2(3H)-benzothiazolone. m.p., 153°-153.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04720297 |
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| Source dataset | uspto-grants-1988_01 |
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| ORD ID | ord-89427ef2d40745fe8755ce8db8a88986 |
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| Source note | uspto-grants-1988_01 |
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