HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Bromomethyl)-2-chloro-4-iodobenzene → N-[(2-chloro-4-iodophenyl)methyl]phthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Bromomethyl)-2-chloro-4-iodobenzene | HCID 22058683 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-[(2-chloro-4-iodophenyl)methyl]phthalimide | HCID 66719866 | 72.2% |
Reaction Steps
In a solution of 7.6 g of 1-bromomethyl-2-chloro-4-iodobenzene in 50 mL of N,N-dimethylformamide, 3.7 g of potassium phthalimide was added, and stirred at room temperature for 1 hour. After the completion of the reaction, the reaction mixture was diluted with 80 mL of ethyl acetate, washed with water (30 mL×2), and then dehydrated with and dried over saturated sodium chloride aqueous solution and anhydrous sodium sulfate in that order, and the solvent was distilled off under reduced pressure to obtain 5.7 g of the aimed product as white crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08242283B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-ff9861bdea4c4a8a9b68eeb9350659f4 |
| Source note | uspto-grants-2012_08 |