Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium ethylxanthate | HCID 2735045 | — |
| Reactant | HCID 178442503 | HCID 178442503 | — |
| Catalyst | 18-Crown-6 | HCID 28557 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178473696 | HCID 178473696 | 80.2% |
Reaction Steps
A stirred solution of 18-Crown-6 (0.03 g) in dry tetrahydrofuran (25 ml) was treated successively with potassium ethylxanthate (0.44 g) and diethyl 3-bromo-3(1-trityl-1,2,4-triazol-3-yl)propane phosphonate (1.0 g, prepared as described in Example 29). The mixture was allowed to stand for two days, poured into water and extracted with ethyl acetate. The extracts were washed with brine, dried over magnesium sulphate, and evaporated under reduced pressure. The residue was chromatographed on silica, using dichloromethane-ethanol (49:1) as eluant, to give diethyl 3(ethoxythiocarbonylthio)-3(1-trityl-1,2,4-triazol-3-yl)propane phosphonate (0.86 g) as a colourless gum. NMR(CDCl3): δ 1.25(6H,m), 1.4(3H,t), 1.7-1.9(2H,m), 2.3-2.4(2H,m), 4.0(4H,m), 4.6(2H,m), 5.05(1H,t), 7.1(6H,m), 7.3(9H,m), 7.9(1H,S). M/S: M+ 609.
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-3662c22e648b423788badc57610c3d2a |
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| Source note | uspto-grants-1999_07 |
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