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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158142Generated: October 31, 2026

Trifluoroacetic acid → 4-Fluoro-N-methyl-benzenepropanamine

https://huagongshe.com/reaction/1158142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant[3-(4-Fluoro-phenyl)-propyl]-methyl-carbamic acid tert-butyl esterHCID 59512610—
SolventDichloromethaneHCID 6344—
Product4-Fluoro-N-methyl-benzenepropanamineHCID 1108426672.5%

Reaction Steps

To a solution of [3-(4-fluoro-phenyl)-propyl]-methyl-carbamic acid tert-butyl ester (0.417 g, 1.560 mmol) in 3 mL of dichloromethane, was added trifluoroacetic acid (3 mL). After stirring at room temperature for 3 h, the reaction mixture was concentrated under reduced pressure. The residue was re-dissolved in 20 mL of ethyl acetate and the resulting solution was washed with NaOH solution (1N) and brine, and dried over anhydrous Na2SO4. Removal of the solvent under reduced pressure provided the title compound as a colorless oil (0.189 g, 72% yield), which was used directly in the next step (Step d of Specific Scheme 7) without further purification. GC-MS: tR=5.6 min; m/z 167 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807720B2
Source datasetuspto-grants-2010_10
ORD IDord-7451f565c6c0429b8b8abb2b9fa91d62
Source noteuspto-grants-2010_10