HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869538Generated: November 3, 2026
Ammonium Acetate → 1-[3-(Trifluoromethoxy)phenyl]ethan-1-amine
https://huagongshe.com/reaction/1869538
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 1-(4-(Trifluoromethoxy)phenyl)ethan-1-one | HCID 522821 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-[3-(Trifluoromethoxy)phenyl]ethan-1-amine | HCID 22605542 | — |
Reaction Steps
An Emrys Process Vial (2-5 ml) was charged with 420 mg (2 mmol) of 1-(4-trifluoromethoxy-phenyl)-ethanone, ammonium acetate in MeOH (4.0 ml of a 5 M solution, 20 mmol) and sodium cyanoborohydride in MeOH (0.440 ml of a 5 M solution, 2.2 mmol). The reaction vessel was sealed and heated to 120° C. for 5 min in an Emrys Optimizer. After cooling and manual release of remaining pressure the vessel was uncapped and the reaction mixture concentrated at reduced pressure. The residue was dissolved in Et2O (10 ml) and extracted with 2 M aqueous HCl (3×5 ml). The combined aqueous phases were adjusted to pH 9 with a 10 M aqueous KOH and extracted with CH2Cl2 (4×10 ml). The combined organic phases were dried over MgSO4 and the solvent evaporated at reduced pressure to afford 1-(3-trifluoromethoxy-phenyl) -ethyl amine which is used as crude product for step 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07638553B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-d69cb1d2b7d5445c8ff6a07a2477005b |
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| Source note | uspto-grants-2009_12 |
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