HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 4-Fluoro-N-methyl-benzenepropanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | [3-(4-Fluoro-phenyl)-propyl]-methyl-carbamic acid tert-butyl ester | HCID 59512610 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Fluoro-N-methyl-benzenepropanamine | HCID 11084266 | 72.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07807720B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-7451f565c6c0429b8b8abb2b9fa91d62 |
| Source note | uspto-grants-2010_10 |