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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728958Generated: October 30, 2026

Sodium Hydroxide → 2-(Methylthio)-1H-imidazole-4,5-dimethanol

https://huagongshe.com/reaction/1728958

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHydrideHCID 166653—
ReactantDiethyl 1-methyl-2-(methylthio)-1H-imidazole-4,5-dicarboxylateHCID 303834—
ReactantAluminium lithium hydrideHCID 21226445—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product2-(Methylthio)-1H-imidazole-4,5-dimethanolHCID 53732353—

Reaction Steps

A solution of the above diethyl 2- (methylthio)-4,5-imidazoledicarboxylate (23 mmol) in freshly distilled anhydrous dichloromethane (50 mL) is added slowly to a stirred suspension of lithium aluminum hydride (69 mmol) in anhydrous ether (140 mL) at 0°-5° C. The mixture is stirred at about 0°-5° C. for about 3 hours after the addition is completed, then for about 1 hour at room temperature. The excess hydride is carefully decomposed by the slow, sequential addition of water (2.6 mL), 15% sodium hydroxide solution (2.6 mL), and water (7.8 mL). The precipitate of inorganic salts is filtered and extracted continuously for about 24 hours with tetrahydrofuran heated under reflux in a Soxhlet apparatus. The tetrahydrofuran solution is combined with the filtrate from the reaction mixture and concentrated to dryness in vacuo. The product is dried in vacuo and crystallized from tetrahydrofuran to give 2-(methylthio)-4,5-bis(hydroxymethyl) imidazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05329012
Source datasetuspto-grants-1994_07
ORD IDord-fa3a6b6d18c84010ae48546a71474d5d
Source noteuspto-grants-1994_07