HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 4-(2-Aminoethyl)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | tert-Butyl 4-cyanophenethylcarbamate | HCID 21955533 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(2-Aminoethyl)benzonitrile | HCID 21912525 | 95.8% |
Reaction Steps
Compound 114 (308 mg, 1.25 mmol) was dissolved in DCM (4 mL) and the solution was cooled in an ice-water bath. TFA (3.5 mL) was then added and the mixture was stirred at room temperature for 15 min. The reaction mixture was concentrated in vacuo and the residue was dissolved in EtOAc (50 mL). The solution was washed with K2CO3 (sat., 3×), brine, dried and concentrated to yield 115 (175 mg, 95%) as a pale yellow oil. MS (APCI): m/z 147 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08541423B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-a766666a5cee47efaed4399655e05a4c |
| Source note | uspto-grants-2013_09 |