HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854673Generated: October 30, 2026
Isopropyl iodide → HCID 58934193, compound
https://huagongshe.com/reaction/854673
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tert-Butyl diethylphosphonoacetate | HCID 2773685 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58934193 | HCID 58934193 | — |
Reaction Steps
5.5 ml of tert-butyl diethylphosphonoacetate are dissolved in 20 ml of dimethylformamide, and 820 mg of sodium hydride (60% strength in paraffin oil) are added a little at a time at 0° C. The suspension is stirred at 0° C. for 15 minutes, and 2.4 ml of isopropyl iodide are then added. The mixture is stirred at room temperature for 12 hours. 250 ml of ethyl acetate are then added, and the reaction mixture is washed three times with in each case 150 ml of water. The organic phase is dried over MgSO4 and concentrated under reduced pressure. The residue is purified on silica gel using the mobile phase n-heptane:ethyl acetate=5:1. This gives 4.2 g of tert-butyl 2-(diethoxyphosphoryl)-3-methylbutyrate as an oil. C13H27O5P (294.33), MS(ESI): 239 (M-C4H8+H+), Rf(n-heptane:ethyl acetate=1:1)=0.34.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07259177B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-4193f7a07e4349de9ffa0cfb3ac240a2 |
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| Source note | uspto-grants-2007_08 |
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