Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | tert-Butyl diethylphosphonoacetate | HCID 2773685 | — |
| Reactant | HCID 178468872 | HCID 178468872 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178468870 | HCID 178468870 | 80.5% |
Reaction Steps
0.682 g of tert-butyl diethylphosphonoacetate (2.7 mmol, 1.1 eq.) is placed in 5 mL of DMF at 4° C. with stirring, 0.065 g of sodium hydride (2.7 mmol, 1.1 eq.) is added. After stirring for 1 hour, 0.64 g of ethyl trans-4-(4-formylcyclohexyl)benzoate (2.46 mmol, 1 eq.) dissolved in 5 mL of DMF is added dropwise. After stirring for 18 hours, 10% potassium hydrogen sulfate solution is added. The reaction medium is extracted twice with ethyl acetate. The organic phases are combined, washed twice with water, washed with brine, dried over sodium sulfate and evaporated. The residue is chromatographed on silica gel with a gradient of ethyl acetate in heptane ranging from 10% to 20%. 0.71 g of ethyl trans-4-[4-((E)-2-tert-butoxycarbonylvinyl)cyclohexyl]benzoate is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546391B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-737ff7aed4df4910bdf67333ac419e00 |
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| Source note | uspto-grants-2013_10 |
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