HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Amino-1,2-propanediol → 5-Cyano-3-[N-(2,3-dihydroxypropyl)carbamoyl]-2,4,6-triiodobenzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Amino-1,2-propanediol | HCID 73561 | — |
| Reactant | 5-Cyano-2,4,6-triiodoisophthalic acid dichloride | HCID 12940840 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-Cyano-3-[N-(2,3-dihydroxypropyl)carbamoyl]-2,4,6-triiodobenzoyl chloride | HCID 12940850 | — |
Reaction Steps
18.1 g of 5-cyano-2,4,6-triiodoisophthalic acid dichloride is combined in 750 ml of dioxane at 80° C. with 7.1 g of 1-amino-2,3-propanediol and stirred for 2 hours. The mixture is then separated from the precipitated hydrochloride of 1-amino-2,3-propanediol, and the filtrate is concentrated under vacuum. The residue is extracted by boiling with 800 ml of ethyl acetate. After concentration and cooling, 11.7 g (59% of theory) of 5-cyano-3-[N-(2,3-dihydroxypropyl)carbamoyl]-2,4,6-triiodobenzoyl chloride is crystallized from the extract as a white powder; mp 285°-288° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04328202 |
| Source dataset | uspto-grants-1982_05 |
| ORD ID | ord-395abb7a6f2d4a97be427b8e03ee2db9 |
| Source note | uspto-grants-1982_05 |