HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloroethanol → HCID 86745333, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloroethanol | HCID 34 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | HCID 86745334 | HCID 86745334 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 86745333 | HCID 86745333 | — |
Reaction Steps
5-Acetamido-N,N'-bis[(2,3-dihydroxypropyl)-2-hydroxyethyl]-2,4,6-triiodoisophthalamide, prepared as in Example 2, Step B, (83.5 g, 0.1 g-mole) is dissolved in 1 N NaOH (140 ml, 0.14 g-mole) and the solution is stirred at room temperature for 1 hour and 2-chloroethanol (13.7 g, 0.17 g-mole) is added. The solution is stirred at 50° C. for 5 hours to complete the reaction. The solution is acidified with H2SO4 and evaporated to dryness under reduced pressure. The residue is triturated with MeOH and the precipitated solid is filtered. The mother liquor is concentrated under vacuum and the crude product is purified by reverse-phase (C18) HPLC to give the purified final product. The yield of this reaction and purification is 80%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05075502 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-e6a7aea994124c7488d549ae0ae70db4 |
| Source note | uspto-grants-1991_12 |