HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 7alpha-(5-Acetoxypentyl)-3,17beta-bis-(tetrahydropyran-2-yloxy)-estra-1,3,5(10)-triene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 70191893 | HCID 70191893 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 7alpha-(5-Acetoxypentyl)-3,17beta-bis-(tetrahydropyran-2-yloxy)-estra-1,3,5(10)-triene | HCID 20683877 | — |
Reaction Steps
5.6 g of crude 7α-(5-acetoxypentyl)-estra-1,3,5(10)-triene-3,17β-diol is dissolved in 35 ml of anhydrous tetrahydrofuran and mixed with 3.5 ml of dihydropyran and 0.18 g of p-toluenesulfonic acid. The mixture is stirred at room temperature overnight, then diluted with ethyl acetate, and the mixture is shaken out in succession with saturated sodium bicarbonate solution and saturated common salt solution. The organic phase is dried with sodium sulfate and concentrated by evaporation in a vacuum, yield 8.31 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06288051B1 |
| Source dataset | uspto-grants-2001_09 |
| ORD ID | ord-2c7fd111ceec4178a1e198cbe9d41cfa |
| Source note | uspto-grants-2001_09 |