Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sesamol | HCID 68289 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | 2,5-Bis(ethylsulfonyl)pyridine | HCID 13278015 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20232716 | HCID 20232716 | 80.8% |
Reaction Steps
Into a reaction flask was weighed 5.6 g of t-BuOK and then 50 ml of THF was added. In 50 ml of DMSO was dissolved 6.2 g of 3,4-methylenedioxyphenol which was then slowly added to the t-BuOK solution with stirring. To the resulting potassium phenate solution was added 10.5 g of 2,5-bis(ethylsulfonyl)pyridine and this mixture heated at 50°-55° C. for 3 hrs. After cooling, the reaction mixture was poured into 400 g of ice, stirred and then filtered. The solid which was recovered was dissolved in CH2Cl2, treated with charcoal, dried over MgSO4 and then filtered. The CH2Cl2 solution was concentrated to 50 ml, diluted with an equal volume of hexane and then chilled and a crystalline material recovered, which provided 9.9 g, (80% yield), of 5-(ethylsulfonyl)-2-(3,4-methylenedioxyphenoxy)pyridine, m.p. 97°-99° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04616087 |
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| Source dataset | uspto-grants-1986_10 |
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| ORD ID | ord-391eac91c0e64ab39fc721fd1b9ef2fd |
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| Source note | uspto-grants-1986_10 |
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