HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Ether 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 | Ether phthalimide | HCID 18959638 | 119.4% |
Reaction Steps
At 20° to 25° C. and over a period of 1 hour, 108 ml of triethylamine was dripped into 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. After the mixture had been kept for 5 hours at 60° C., the cold mixture was poured into 2000 ml of ice water, the precipitate was suction filtered, washed with water and isopropanol and dried under reduced pressure over phosphorus pentoxide. There was obtained 185 g (82%) of phthalimide ether, m.p. 62°-64° C. 1H-NMR (250 MHZ, d6 -DMSO): δ=3.85 (m,2H), 4.35 (m,2H), 4.54 (s,2H), 7.10-7.40 (m,4H), 7.88 (s,4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05190573 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-a43b7d7b3ae14491b541658f6815adb3 |
| Source note | uspto-grants-1993_03 |