HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514829Generated: October 25, 2026
2-Fluoro-6-nitroaniline → 2-Fluoro-6-nitrophenylthiocyanate
https://huagongshe.com/reaction/514829
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Fluoro-6-nitroaniline | HCID 87316 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 2-Fluoro-6-nitrophenylthiocyanate | HCID 90419022 | 99.9% |
Reaction Steps
A solution of 2-fluoro-6-nitroaniline (3 g, 0.02 mol) in conc. sulphuric acid (30 mL) and water (30 mL) was diazotized at 0-3° C. for 90 min with aqueous sodium nitrite (1.45 g, 0.021 mol). After addition of potassium thiocyanate (2.522 g, 0.026 mol) in water (10 mL), the diazo-liquor was stirred vigorously into a suspension of cuprous thiocyanate (6.05 g, 0.05 mol) in water (20 mL) at 5° C. After stirring at 5° C. for 2 hr, the mixture was then heated at 70° C. for 20 min, then was cooled overnight, filtered, and the cake extracted with EtOAc to get the crude product (3.96 g) which was used in the next step without further purification. LC-MS: m/z 199.2 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09108921B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-522fe75e085945588571e3fc32547aab |
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| Source note | uspto-grants-2015_08 |
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