HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 2-Iodo-1-[2-[(2-methoxyphenoxy)methyl]-3-thiazolidinyl]ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | HCID 10447619 | HCID 10447619 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Iodo-1-[2-[(2-methoxyphenoxy)methyl]-3-thiazolidinyl]ethanone | HCID 10385874 | 75.7% |
Reaction Steps
A solution of 3-α-chloroacetyl-2-(o-methoxyphenoxy)methyl-thiazolidine (6 g) in acetone (80 ml) is heated to reflux temperature in the presence of sodium iodide (5 g) for 3 hours and then poured in ice and water (400 ml). The precipitate is collected, dissolved in methylene dichloride and washed with water, 5% aqueous NaHCO3, 2N sodium thiosulphate, water and dried on Na2SO4. After the usual work-up, the residue is crystallized from acetone and isopropanol to give 5.92 g of 3-α-iodoacetyl-2-(o-methoxyphenoxy)methyl-thiazolidine m.p. 81°-83° C. Using this procedure sodium bromide, the 3-α-bromoacetyl-2-(o-methoxyphenoxy)methyl-thiazolidine is obtained, m.p. 82°-84° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04857643 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-fab2b065c09e4cecb1382ab3e0989764 |
| Source note | uspto-grants-1989_08 |