HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Fluorophenethylamine → N-Benzyloxycarbonyl-2-(parafluorophenyl)ethylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Fluorophenethylamine | HCID 4653 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-Benzyloxycarbonyl-2-(parafluorophenyl)ethylamine | HCID 23366829 | 46% |
Reaction Steps
Benzylchloroformate (12.2 g, 72 mmol) was added dropwise to a stirred solution, at 0° C., of 4-fluorophenylethyl amine (9.42 g, 72 mmol) in 50 mL of DMF. The mixture was stirred for an additional 3 hours at the same temperature. The reaction was quenched with water and extracted with 3×100 mL of ethyl acetate. The combined ethyl acetate extracts were washed with 2×100 mL of 5% HCl, water and dried, over Na2SO4. Evaporation of the solvent resulted in a yellowish solid which was purified by recrystallization from ethyl acetate-hexane to furnish 8.6 g (46% yield) of N-Benzyloxycarbonyl-2-(para-fluorophenyl)ethylamine. mp 51°-52° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05580878 |
| Source dataset | uspto-grants-1996_12 |
| ORD ID | ord-9fbbbc6c0e254087b8eada6d4394d3f0 |
| Source note | uspto-grants-1996_12 |