Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | HCID 14013943 | HCID 14013943 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 14013946 | HCID 14013946 | 11% |
Reaction Steps
A mixture of 3 g (0.009 mol) of product of Example 201 and 7.28 g (0.018 mol) of Lawesson's reagent in 100 ml of toluene was refluxed for 16 days. The reaction mixture was cooled to 25° C., poured into H2O, and extracted with ethyl acetate. The organic phase was dried (MgSO4), and concentrated in vacuo to 1.4 g of a brown oil. Chromatography using 10% ethyl acetate/cyclohexane as an eluting solvent afforded 0.35 g (11%) of product as a beige solid: mp 129°-131° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04921530 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-09a4c2730b30462a97c463e269126ba0 |
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| Source note | uspto-grants-1990_05 |
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