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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
Reactant1-(4-(Trifluoromethoxy)phenyl)ethan-1-oneHCID 522821—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
Product1-[3-(Trifluoromethoxy)phenyl]ethan-1-amineHCID 22605542—

Reaction Conditions

Temperature120 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07638553B2
Source datasetuspto-grants-2009_12
ORD IDord-d69cb1d2b7d5445c8ff6a07a2477005b
Source noteuspto-grants-2009_12