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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957376Generated: November 2, 2026

Methyl iodide → (4R)-4,5-Dihydro-2-(methylthio)-4-thiazolemethanol

https://huagongshe.com/reaction/1957376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178521049HCID 178521049—
SolventMethanolHCID 887—
Product(4R)-4,5-Dihydro-2-(methylthio)-4-thiazolemethanolHCID 2286234959%

Reaction Steps

To a mixture solution of 4.88 g of 4(R)-hydroxymethyl-2-mercapto-1,3-thiazoline [Compound (5)] and 22.8 ml of diisopropylethylamine in 65 ml of dry methanol was added 14.00 g of methyl iodide under refluxing condition, and the reaction mixture was refluxed for 1 hour. After removal of the solvent under reduced pressure, the resulting residue was dissolved in ethyl acetate and the organic layer was washed with saturated sodium bicarbonate solution, water and saturated saline solution and dried over magnesium sulfate. The solvent was removed under reduced pressure and the resulting residue was purified by silica gel column chromatography (chloroform-acetone) to give 3.14 g (59%) of 4(R)-hydroxymethyl-2-methylthio-1,3-thiazoline [Compound (6)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05783703
Source datasetuspto-grants-1998_07
ORD IDord-060f4bd975894dc8a351c241cc99c3fa
Source noteuspto-grants-1998_07