Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1,1-bis(5-chloropyrid-2-yl)-2-(1H-1,2,4-triazol-1-yl)ethanol | HCID 20274516 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Hydrochloric Acid | HCID 313 | — |
| Product | 1,1-Bis(5-chloropyrid-2-yl)-2-(1H-1,2,4-triazol-1-yl)ethyl chloride hydrochloride | HCID 20274513 | — |
Reaction Steps
To 2.0 g (5.95 mmoles) of 1,1-bis(5-chloropyrid-2-yl)-2-(1H-1,2,4-triazol-1-yl)ethanol and 2.4 g (35.3 mmoles) of imidazole in 60 ml. of acetonitrile was added with stirring 2.1 g (17.65 mmoles) of thionyl chloride, the reaction mixture stirred for 2 hrs at room temperature and the solvent allowed to evaporate. Dilute sodium bicarbonate solution (30 ml) was added to the residue and the mixture extracted with ethyl acetate (3×50 ml). The combined extracts were dried over magnesium sulfate, concentrated to dryness and the residue chromatographed on 230-400 mesh silica gel using ethyl acetate-petrol (b.p. 60°-80° C.) (1:1, v:v) as the eluent. The fractions containing the product were combined and concentrated in vacuo to a colorless oil. Treatment of the residue with ethereal hydrogen chloride gave 1.4 (60% yield) of the desired product as a white solid, m.p. 115°-125° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04529799 |
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| Source dataset | uspto-grants-1985_07 |
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| ORD ID | ord-a5f38b363df24986a56597c5a0a3ab84 |
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| Source note | uspto-grants-1985_07 |
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