HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 5-Amino-2,4,6-triiodoisophthaloyl dichloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 5-Amino-2,4,6-triiodo-1,3-benzenedicarboxylic acid | HCID 3015783 | — |
| Reactant | 1H-Imidazolium, 2-chloro-4,5-dihydro-1,3-dimethyl-, chloride | HCID 10986715 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 5-Amino-2,4,6-triiodoisophthaloyl dichloride | HCID 9894858 | 95% |
Reaction Steps
To a reaction flask, 4.23 g (0.025 mole) of 2-chloro-1,3-dimethylimidazolinium chloride, 5.58 g (0.01 mole) of 5-amino-2,4,6-triiodoisophthalic acid and 80 g of toluene were charged and reacted at 105°-110° C. for 4 hours. Thereafter, the reaction mass was cooled and toluene was removed under reduced pressure. To the concentrate thus obtained, 100 ml of hexane was added to crystallize 5-amino-2,4,6-triiodoisophthaloyl dichloride. The precipitate was filtered and dried under reduced pressure to obtain 5.65 g (95% yield) of 5-amino-2,4,6-triiodoisophthaloyl dichloride as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05750779 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-5d5d0b90f425497b8b534eb2e05a9523 |
| Source note | uspto-grants-1998_05 |