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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1685214Generated: November 3, 2026

Triphenylphosphine → 2-Amino-1-(4-fluoro-3-(trifluoromethyl)phenyl)ethanone

https://huagongshe.com/reaction/1685214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantSodium AzideHCID 33557—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant2-Bromo-4'-fluoro-3'-(trifluoromethyl)acetophenoneHCID 2778787—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-Amino-1-(4-fluoro-3-(trifluoromethyl)phenyl)ethanoneHCID 56971690150.4%

Reaction Steps

Cool a solution of 2-bromo-1-(4-fluoro-3-(trifluoromethyl)phenyl)ethanone (93% pure by HPLC, 1000 g; 3.51 mol) and THF (5 L) to <5° C. in an ice bath. Add a solution of sodium azide (239 g; 3.68 mol, 1.05 eq) in water (800 mL) drop wise over one hour at <5° C. After stirring at <5° C. for one hour, separate and discard the aqueous layer. While still cold, add the organic layer slowly over 3 hours to a solution of triphenylphosphine (920.2 g, 3.51 mol, 1.0 eq), p-toluenesulfonic acid monohydrate (1335 g, 7.02 mol, 2.0 eq), and THF (5 L). Maintain the temperature at <15° C. throughout this addition and solids precipitate during the addition. Stir the reaction mixture at <20° C. for 2 hours and then filter the solid, wash with THF (3×2 L), and dry at 50° C. under vacuum to give 1167.4 g (85%, 92% corrected for starting material purity) of 2-amino-1-(4-fluoro-3-(trifluoromethyl)phenyl)ethanone, 4-methylbenzenesulfonate as a white crystalline solid. HRMS (ESI) m/z (M+H) 222.0531 calculated for C9H8F4NO 222.0537

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148387B2
Source datasetuspto-grants-2012_04
ORD IDord-c1de731336fa44d8ad91fdbd604683b1
Source noteuspto-grants-2012_04