Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl p-toluenesulfonate | HCID 6645 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 10451669 | HCID 10451669 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 11143440 | HCID 11143440 | 71.4% |
Reaction Steps
2.58 g (7.0 mmol.) of (R)-3-t-butyldimethylsilyloxy-6-dimethoxyphosphinyl-5-oxohexanoic acid was dissolved in 16 ml of acetone. To the acetone solution were added 6.52 g (35 mmol.) of methyl p-toluenesulfonate and 1.06 g (7.7 mmol.) of potassium carbonate, and the resulting mixture was vigorously stirred for 6 hours at room temperature to give a reaction solution. The reaction solution was mixed with 16 ml of water and then extracted with 20 ml of toluene. The toluene portion was dried over anhydrous magnesium sulfate and concentrated to give an oil. The oil was treated by column chromatography (eluent: ethyl acetate) to give 1.91 g (5.0 mmol.) of methyl (R)-3-t-butyldimethylsilyloxy-6-dimethoxyphosphinyl-5-oxohexanoate as an oil (yield: 71%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05717124 |
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| Source dataset | uspto-grants-1998_02 |
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| ORD ID | ord-5ca7102e85a442c58bd7a52cf8c6211a |
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| Source note | uspto-grants-1998_02 |
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