HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672616Generated: November 1, 2026
Formic Acid → Methyl 4-[2-carboxy-4-(4-cyanophenyl)butyl]benzoate
https://huagongshe.com/reaction/1672616
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 57831389 | HCID 57831389 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Methyl 4-[2-carboxy-4-(4-cyanophenyl)butyl]benzoate | HCID 57831396 | 82.2% |
Reaction Steps
A solution of 41.8 ml (0.3 mol) of triethylamine and 8.6 ml (0.23 mol) of formic acid in 500 ml of dioxane is added to a solution of 43.5 g (0.09 mol) of diallyl 2-[2-(4-cyanophenyl)ethyl]-2-(4-methoxycarbonylbenzyl)malonate from Example 13A, 1.67 g (0.01 mol) of triphenylphosphine and 410 mg of palladium acetate in 505 ml of dioxane at room temperature. The reaction mixture is then stirred at 100° C. for 2 hours. After conversion is complete, the reaction solution is cooled and the solvent is removed in vacuo. The resulting residue is purified by flash chromatography on silica gel (mobile phase: dichloromethane/methanol 50:1). 25 g (0.074 mol, 82% yield) of a colorless solid are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07998988B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-396ab65cec49441591d087d6560a2778 |
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| Source note | uspto-grants-2011_08 |
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