HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-[2-(2-Fluorobenzyloxy)-ethoxy]-phthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-Hydroxyphthalimide | HCID 10665 | — |
| Reactant | 1-Bromo-2-(2-fluorobenzyloxy)-ethane | HCID 23353097 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | N-[2-(2-Fluorobenzyloxy)-ethoxy]-phthalimide | HCID 23353096 | 82% |
Reaction Steps
108 ml of triethylamine were added dropwise to a mixture of 165 g (0.71 mol) of 1-bromo-2-(2-fluorobenzyloxy)-ethane, 116 g (0.7 mol) of N-hydroxyphthalimide and 710 ml of N-methyl-2-pyrrolidone at from 20° to 25° C. in the course of 1 hour. After 5 hours at 60° C. the cold reaction mixture was poured into 200 ml of ice water and the precipitate was filtered off under suction, washed with water and isopropanol and dried under reduced pressure over phosphorus pentoxide. Yield: 82%; mp.: 62°-64° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05597776 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-10e77219ba014318ab6b6f4538433549 |
| Source note | uspto-grants-1997_01 |