HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238952Generated: October 29, 2026
Hydrochloric Acid → 2-(Difluoromethyl)-4-fluoroaniline
https://huagongshe.com/reaction/238952
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-(Difluoromethyl)-4-fluoro-1-nitrobenzene | HCID 46311787 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(Difluoromethyl)-4-fluoroaniline | HCID 58482996 | 60.1% |
Reaction Steps
Under a nitrogen atmosphere, to a solution of the above 2-(difluoromethyl)-4-fluoro-1-nitrobenzene (5.9 g, 31 mmol) in ethanol (0.10 L), stannous chloride dihydrate (28 g, 0.12 mol) and concentrated hydrochloric acid (20 mL) were successively added under ice-cooling, and the mixture was stirred at room temperature for 1 hour. After the reaction, ethanol was distilled off under reduced pressure and a 5M aqueous sodium hydroxide solution was added under ice-cooling to make it basic. Thereafter, it was extracted with diethyl ether and after it was successively washed with water and saturated brine, it was dried with sodium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane, 1:4, v/v) to give the title compound (3.0 g, 60%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642640B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-e806954345ab4dea98e0acc0a1d25fed |
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| Source note | uspto-grants-2014_02 |
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