HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Methyl(E)-8-(2-{[tert-butyl(dimethyl)silyl]oxy}phenyl)-6-oxo-7-octenoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Benzaldehyde, 2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]- | HCID 10900635 | — |
| Reactant | Methyl 7-(diethoxyphosphoryl)-6-oxoheptanoate | HCID 15546840 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl(E)-8-(2-{[tert-butyl(dimethyl)silyl]oxy}phenyl)-6-oxo-7-octenoate | HCID 23118874 | — |
Reaction Steps
Under argon, 0.26 g (10.87 mmol) of sodium hydride was added to a solution of 3.20 g (10.87 mmol) of methyl 7-(diethoxyphosphoryl)-6-oxoheptanoate from Ex. XIIb in 53 ml of THF. The mixture was stirred at room temperature for 30 min, a solution of 9.06 mmol of 2-{[tert-butyl(dimethyl)silyl]oxy}benzaldehyde from Ex. XIIa in 20 ml of THF was added and the mixture was stirred at room temperature for 18 h. Water was added, the mixture was extracted with ethyl acetate, the combined organic phases were dried over Na2SO4 and the solvent was removed. The product was purified chromatographically (silica gel, cyclohexane/EA 10:1). This gave 2.51 g (67.8%) of a colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07674825B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-0f6a3a0ad00d462191566b2cd05e80cd |
| Source note | uspto-grants-2010_03 |