HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46484Generated: October 27, 2026
Ethanol → 2-(5-Methyl-4-imidazolylmethylthio)ethanol
https://huagongshe.com/reaction/46484
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Mercapto-ethanol | HCID 4713212 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 178433265 | HCID 178433265 | — |
| Product | 2-(5-Methyl-4-imidazolylmethylthio)ethanol | HCID 12797273 | — |
Reaction Steps
Sodium (3.0 g) was added, with stirring under nitrogen, to dry ethanol (75 ml). After the sodium had dissolved mercaptoethanol (9.0 ml) was introduced and to this mixture was added 4-methyl-5-chloromethylimidazole hydrochloride (10 g), as a solid, over a period of 1.5 hours at room temperature. The mixture was then stirred for a further 1 hour at room temperature. After this time the reaction was warmed and the ethanol distilled off at reduced pressure. The residue was taken up in water, acidified with concentrated hydrochloric acid, and continuously extracted with ether to remove the excess mercaptoethanol. The aqueous fraction was then basified using solid sodium carbonate and continuously extracted with ethyl acetate. To the extract was added a further volume of ethyl acetate and the whole warmed to re-dissolve the crude product which had deposited. After drying (MgSO4) and reducing the volume, crystallisation from this solution below 40° and cooling to -15° afforded 2-(5-methyl-4-imidazolylmethylthio)ethanol, m.p. 74°-76°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04173644 |
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| Source dataset | uspto-grants-1979_11 |
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| ORD ID | ord-c06f9a2815df4dcea4d090ae8316266a |
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| Source note | uspto-grants-1979_11 |
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