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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | ethyl 4-(ethylthio)-2-methyl-1H-imidazole-5-carboxylate | HCID 10130590 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(ethylthio)-2-methyl-1H-imidazole-5-methanol | HCID 21479011 | 76.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05412101 |
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| Source dataset | uspto-grants-1995_05 |
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| ORD ID | ord-491467a9de264eb1927f75ff0f8550d4 |
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| Source note | uspto-grants-1995_05 |
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