Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 86733058 | HCID 86733058 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 68135586 | HCID 68135586 | — |
Reaction Steps
trans-2-(4-Cyclohexyl-3-hydroxy-1-butenyl)-5-[(tetrahydropyran-2-yl)oxy]cyclopentaneheptanoic acid methyl ester acetate (44 g), described in Example 8, is dissolved in acetic acid (426 ml), water (212 ml) and tetrahydrofuran (35.7 ml). The mixture is stirred at 60°C (bath temperature) for 3 hr. The solvent is removed under reduced pressure. The residue is taken up in ether. The ether solution is washed with water, dried and evaporated to yield trans-2-(4-cyclohexyl-3-acetoxy-1-butenyl)-5-hydroxycyclopentaneheptanoic acid methyl ester νmaxCHCl3 3,451, 1,730, 1,240 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US03937801 |
|---|
| Source dataset | uspto-grants-1976_02 |
|---|
| ORD ID | ord-542d552642a64a32bbe6d264d4087b49 |
|---|
| Source note | uspto-grants-1976_02 |
|---|