HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714539Generated: October 29, 2026
Isopropyl iodide → Methyl 3-cyano-4-isopropoxybenzoate
https://huagongshe.com/reaction/1714539
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 3-cyano-4-hydroxybenzoate | HCID 11769089 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 3-cyano-4-isopropoxybenzoate | HCID 21956805 | 100% |
Reaction Steps
To a solution of methyl 3-cyano-4-hydroxybenzoate (82 g, 463 mmol; J. Med. Chem, 2002, 45, 5769) in dimethylformamide (800 mL) was added 2-iodopropane (93 mL, 926 mmol) and potassium carbonate (190 g, 1.4 mol). The resulting mixture was heated at 50° C. for 16 h, at which time it was allowed to cool to room temperature. The reaction was filtered and the mother liquor diluted with 0.5 N sodium hydroxide (1 L). The resulting mixture was extracted with ether (2×1 L) and the organics washed with 1 N HCl (1 L) and brine (700 mL), dried (MgSO4) and concentrated to give 100 g (˜100%) of methyl 3-cyano-4-[(1-methylethyl)oxy]benzoate as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07795448B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-a5b4d6f657114c6bba8b02a4eda3417d |
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| Source note | uspto-grants-2010_09 |
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