HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Chloromethyl)-4-(4-phenylbutoxy)benzene → N-[p-(4-phenylbutoxy)benzyl]phthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Chloromethyl)-4-(4-phenylbutoxy)benzene | HCID 15115532 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-[p-(4-phenylbutoxy)benzyl]phthalimide | HCID 14881544 | 109.9% |
Reaction Steps
A solution of 1.20 g of p-chloromethyl-(4-phenylbutoxy)benzene and 1.15 g of potassium phthalimide in 20 ml of N,N-dimethylformamide was stirred at 100° C. for 3 hours. The reaction mixture was diluted with ethyl acetate, and the dilution was washed with three portions of water and then with saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residual solid was recrystallized from ethyl acetate to give 1.85 g of N-[p-(4-phenylbutoxy)benzyl]phthalimide. Melting point 106°-107.5° C. ##STR32##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04987132 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-a4b2c6320646427a978917fb0471796d |
| Source note | uspto-grants-1991_01 |