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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722832Generated: November 1, 2026

Sodium Iodide → 2-Iodo-1-[2-[(2-methoxyphenoxy)methyl]-3-thiazolidinyl]ethanone

https://huagongshe.com/reaction/1722832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantHCID 10447619HCID 10447619—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product2-Iodo-1-[2-[(2-methoxyphenoxy)methyl]-3-thiazolidinyl]ethanoneHCID 1038587475.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04857643
Source datasetuspto-grants-1989_08
ORD IDord-fab2b065c09e4cecb1382ab3e0989764
Source noteuspto-grants-1989_08