HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436143Generated: November 3, 2026
Sodium hydride → tert-butyl(S)-5-(tert-butyldiphenylsilanyloxy)-2-(diethoxyphosphoryl)-4-methylvalerate
https://huagongshe.com/reaction/1436143
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tert-Butyl diethylphosphonoacetate | HCID 2773685 | — |
| Reactant | ((R)-3-bromo-2-methylpropoxy)-tert-butyldiphenylsilane | HCID 69007455 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-butyl(S)-5-(tert-butyldiphenylsilanyloxy)-2-(diethoxyphosphoryl)-4-methylvalerate | HCID 86612619 | 52.2% |
Reaction Steps
A solution tert-butyl diethylphosphonoacetate (64 g) in THF (100 mL) was added dropwise to a suspension of sodium hydride (containing 40% mineral oil, 13.2 g) in THF (400 mL) under ice-cooling, and the reaction mixture was stirred at room temperature for 75 minutes. A solution of ((R)-3-bromo-2-methylpropoxy)-tert-butyldiphenylsilane (99.4 g) in THF (100 mL) was added dropwise to the reaction mixture, which was then heated under reflux for 23 hours. Ice water was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (elution solvent: heptane-ethyl acetate system) to obtain 74.6 g of the title compound. The property values of the compound are as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07618960B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-1654b09c28da4899893691a459f8fdb1 |
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| Source note | uspto-grants-2009_11 |
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