Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2041143Generated: November 3, 2026

Ammonia → 4-(2-Fluorophenoxy)benzenemethanamine

https://huagongshe.com/reaction/2041143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantEthanolHCID 702—
ReactantHCID 28411324HCID 28411324—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
Product4-(2-Fluorophenoxy)benzenemethanamineHCID 1957671479%

Reaction Conditions

Temperature60 °C

Reaction Steps

Add 4-(2′-fluorophenoxy)-benzonitrile (1.5 g, 7.0 mmol) and ethanol wet Raney® activated nickel (0.4 g) to a Parr pressure vessel. Immediately add a 7N solution of ammonia in methanol (170 mL) and seal the vessel. Purge the reaction vessel with nitrogen, pressurize the reaction mixture with hydrogen (3400 KPa), seal the vessel, agitate the reaction and heat to 60° C. Continue the reaction for 18 h, turn off the heat and allow the reaction mixture to cool to ambient temperature. Vent the excess hydrogen from the vessel and purge the vessel with nitrogen. Filter the reaction mixture to remove the Raney® nickel. Concentrate in vacuo and purify by chromatography on silica gel eluting with DCM/2M ammonia in methanol (9:1) to obtain the title compound (1.2 g, 79%). MS (ES+) m/z: 201 (M+H—NH3)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580780B2
Source datasetuspto-grants-2013_11
ORD IDord-12eb194e329347e092dc021d8dac6e48
Source noteuspto-grants-2013_11