Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pivalic acid | HCID 6417 | — |
| Reactant | HCID 19046306 | HCID 19046306 | — |
| Reactant | Triethylorthoaceate | HCID 21875354 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 131719271 | HCID 131719271 | — |
Reaction Steps
A solution of 1-[2-(4-tert-butyldimethylsilyloxy-1,3-dihydro -6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-1-hydroxyeth-1-yl]cyclopent-1-ene (0.22 g) in triethylorthoacetate (10 ml) was treated with pivalic acid (0.010 g) and then heated to 100° C., and maintained at that temperature for 18 hours. After cooling to ambient temperature, the solution was diluted with 1:1 ethyl acetate:hexanes and washed sequentially with water, saturated aqueous sodium bicarbonate, and brine. Drying over magnesium sulfate was followed by evaporation; chromatography of the residue on silica gel (10% ethyl acetate in hexanes) afforded ethyl (E) 2-[2-[2-[4-tert-butyldimethylsilyloxy-1,3-dihydro-6-methoxy-7-methyl-3-oxo-isobenzofuran-5-yl]ethylidene]-cyclopent-1-yl]acetate (0.11 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05633279 |
|---|
| Source dataset | uspto-grants-1997_05 |
|---|
| ORD ID | ord-0b6617e9cfd7449aaea81f512395c478 |
|---|
| Source note | uspto-grants-1997_05 |
|---|