HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582172Generated: October 30, 2026
Thionyl Chloride → HCID 178443586, compound
https://huagongshe.com/reaction/582172
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 178444075 | HCID 178444075 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 178443586 | HCID 178443586 | — |
Reaction Steps
Thionyl chloride (20 ml) was added dropwise to a stirred solution of diethyl 3-hydroxy-3(1-trityl-1,2,4-triazol-3-yl)propane phosphonate (1.0 g, prepared as described in Example 24) in pyridine (10 ml), whilst maintaining the temperature below 5° C. The mixture was allowed to warm to room temperature, stirred for three hours, then evaporated under reduced pressure. The residue was dissolved in ethyl acetate, washed with water and brine, dried over magnesium sulphate and evaporated under reduced pressure. This residue was chromatographed on silica, using dichloromethane-ethanol (49:1) as eluant, to give diethyl 3-chloro-3(1-trityl-1,2,4-triazol-3-yl)propane phosphonate (0.64 g, m.p. 123-124° C.). NMR (CDCl3): δ 1.3(6H,t), 1.8-2.1(2H,m), 2.4-2.6(2H,m), 4.1(4H,m), 5.1(1H,t), 7.1(6H,m), 7.4(9H,m), 7.95(1H,s). M/S: M+ 523,525.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05922644 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-04d991e8703a4fa785547410b69282b8 |
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| Source note | uspto-grants-1999_07 |
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