Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 86749426 | HCID 86749426 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86749425 | HCID 86749425 | 93% |
Reaction Steps
A solution of (S,E)-3-[[(1,1-Dimethylethyl)diphenylsilyl]-oxy]-4-[[2-[4-(4-fluorophenyl)-2-(1-methylethyl)-3-quinolinyl]ethenyl]methoxyphosphinyl]butanoic acid, methyl ester (1.136 gm, 1.57 mmol) in THF (14 ml) was treated with HOAc (450 ul, 472 mg, 7.9 mmol) and tetra-n-butylammonium fluoride (1.0M in THF, 5.40 ml, 5.40 mmol). After stirring at room temperature for 18 hours, the solution was poured into saturated NaHCO3 and extracted with EtOAc. The EtOAc extract was washed with brine, dried (Na2SO4), filtered, and stripped to give an oil which was subsequently chromatographed (flash, Merck SiO2, 1:1 acetone: hexane). (S,E)-4-[[2-[4-(4-Fluorophenyl)-2-(1-methyl-ethyl)-3-quinolinyl]-ethenyl]methoxyphosphinyl]3-hydroxybutanoic acid, methyl ester(709 mg, 93%) was obtained as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05686433 |
|---|
| Source dataset | uspto-grants-1997_11 |
|---|
| ORD ID | ord-1da8c38051094ea9b0a2a3a52ab4c0f3 |
|---|
| Source note | uspto-grants-1997_11 |
|---|