HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257475Generated: November 2, 2026
Acetonitrile → 2-Amino-1-(3-(trifluoromethyl)phenyl)ethan-1-one hydrochloride
https://huagongshe.com/reaction/1257475
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 2-Bromo-1-[3-(trifluoromethyl)phenyl]ethan-1-one | HCID 2778386 | — |
| Reactant | Ethanol hydrochloride | HCID 21887872 | — |
| Product | 2-Amino-1-(3-(trifluoromethyl)phenyl)ethan-1-one hydrochloride | HCID 13365885 | — |
Reaction Steps
A mixture of 2-bromo-1-[3-(trifluoromethyl)phenyl]ethanone (22 g), NaN(CHO)2 (9.5 g) and acetonitrile (50 mL) was stirred at room temperature for 3 hr and at 70° C. overnight, and the insoluble material was removed by filtration. The filtrate was concentrated to give an oil. The oil was dissolved in hydrogen chloride-ethanol, and the mixture was stirred at room temperature for 48 hr. The resulting precipitate was collected by filtration, and washed with ether to give the title compound (2.7 g) as a solid. The filtrate was concentrated, and the residue was dissolved in water. The aqueous layer was washed with ether, and the solvent was evaporated under reduced pressure to give the title compound (7.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08461348B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-ffe966b405dc45eab18d49215c5de570 |
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| Source note | uspto-grants-2013_06 |
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