HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54310Generated: October 27, 2026
Ammonia → 2,3,4,5-Tetrafluoro-6-nitroaniline
https://huagongshe.com/reaction/54310
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Pentafluoronitrobenzene | HCID 70154 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2,3,4,5-Tetrafluoro-6-nitroaniline | HCID 2775760 | — |
Reaction Steps
2-Nitro-3,4,5,6-tetrafluoroaniline was prepared using an adaptation of the method of Brooke et al., J. Chem. Soc. 802 (1961). Ammonia gas was bubbled through a solution of pentafluoronitrobenzene (3.00 g, 114.1 mmol) in 200 mL anhydrous diethyl ether for 4 h. During this time the color changed from clear white to a deep yellow and a white precipitate formed. The precipitate (ammonium fluoride) was separated by vacuum filtration and washed with ether (30 mL). The filtrate was rotary evaporated and the resulting orange crystals gave 3 spots on TLC (alumina, benzene). Purification of this sample was achieved by column chromatography (basic alumina, benzene). Purification of this sample was achieved by column chromatography (basic alumina, activity 11) on a 1.5"×20" column. The first band was collected and concentrated to yield a yellow solid 1.88 g (63.0%), mp 44.5-45 (lit. 42.5°-43.5° C.). 19F NMR (C6F6 external standard, δ-162.9) δ-149.9(m), -1.56.6(m), -162.0 (m), -178.3(m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05622952 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-b32d1719e29c4023b0c90e66a8f3e463 |
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| Source note | uspto-grants-1997_04 |
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