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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36017Generated: October 29, 2026

Water → 4-(ethylthio)-2-methyl-1H-imidazole-5-methanol

https://huagongshe.com/reaction/36017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAcetyl chlorideHCID 6367—
Reactantethyl 4-(ethylthio)-2-methyl-1H-imidazole-5-carboxylateHCID 10130590—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
Product4-(ethylthio)-2-methyl-1H-imidazole-5-methanolHCID 2147901176.4%

Reaction Steps

11.64 cm3 of a 1.2M solution of diisobutylaluminium hydride in toluene is added over 10 minutes at -70° C. to a solution of 1 g of ethyl 4-(ethylthio)-2-methyl-1H-imidazole-5-carboxylate (obtained as in Preparation 1 using, in Stage B, acetyl chloride instead of pentanoyl chloride) in 100 cm3 of methylene chloride. The mixture is agitated for 3 hours at ambient temperature then hydrolyzed by the addition of 1 cm3 of water. After agitation for 15 minutes, then filtering, the insoluble part is washed with 20 cm3 of methylene chloride then 5 times with 20 cm3 of a methylene chloride--methanol mixture (9-1). After drying, the filtrate is brought to dryness under reduced pressure. The residue (760 mg) is impasted in 7.6 cm3 of methylene chloride and 614 mg of the expected product is obtained. M.p.=153° C. IR Spectrum: Absence >C=O Absorption OH/NH complex region Heteroaromatic 1582 cm-1 -1524 cm-1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05412101
Source datasetuspto-grants-1995_05
ORD IDord-491467a9de264eb1927f75ff0f8550d4
Source noteuspto-grants-1995_05