HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phthalic Anhydride → HCID 53649200, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Allyloxy-4-chloro-2-fluoroaniline | HCID 13272926 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 53649200 | HCID 53649200 | — |
Reaction Steps
A mixture of 20.2 g of 19A and 14.8 g of phthalic anhydride in 300 mL of toluene was treated with 1.01 g of triethylamine and heated to reflux for 16 hours with a Dean-stark trap to effect azeotropic removal of water. The toluene was removed in vacuo, the residue was dissolved in 800 mL of methylene chloride, and treated with 35 g charcoal. After filtration through celite and concentration of solvent in vacuo, the residue was recrystallized from ethanol to afford N-[3-(allyloxy)-4-chloro-6-fluorophenyl]phthalimide (41A) as tan crystals, m.p.: 148°-150° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05053071 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-2d08cf458c1247ed8346f5e1f2c47d4f |
| Source note | uspto-grants-1991_10 |