HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307411Generated: October 26, 2026
Hydrochloric Acid → 1-[3-(Trifluoromethoxy)phenyl]ethan-1-amine
https://huagongshe.com/reaction/2307411
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 1-(3-(Trifluoromethoxy)phenyl)ethanone | HCID 737161 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-[3-(Trifluoromethoxy)phenyl]ethan-1-amine | HCID 22605542 | 63% |
Reaction Steps
A mixture of 3-trifluoromethoxyacetophenone, oxime, Preparation 14 (3.08 g, 12.36 mmol), Raney nickel (1 mL) in methanol (50 mL) and ammonium hydroxide (5 mL) was hydrogenated (H2, 50 psi) for 16 hours. The reaction mixture was filtered through Celite and the resultant filtrate was concentrated in vacuo. The suspension obtained was acidified with hydrochloric acid (6N) (100 mL). The aqueous layer was washed with diethyl ether (2×50 mL). The aqueous layer was then made basic with sodium hydroxide (10 N) (with cooling). The basic aqueous layer was then extracted with CH2Cl2 (2×100 mL). The combined organic layer was washed with brine (100 mL), dried over anhydrous magnesium sulfate, filtered, and the resultant filtrate was concentrated in vacuo to provide the title compound (1.82 g, 63%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06831080B2 |
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| Source dataset | uspto-grants-2004_12 |
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| ORD ID | ord-eb32b82caf86481c81356f2f43200a77 |
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| Source note | uspto-grants-2004_12 |
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