HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-Isopropyl 4-methylpent-4 enoic acid, alpha-cyano-3 phenoxybenzyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | alpha-Cyano-3-phenoxybenzyl bromide | HCID 12713810 | — |
| Reactant | 4-Methyl-2-propan-2-ylpent-4-enoic acid | HCID 14910859 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-Isopropyl 4-methylpent-4 enoic acid, alpha-cyano-3 phenoxybenzyl ester | HCID 131710868 | — |
Reaction Steps
A mixture of 2-isopropyl-4-methylpent-4-enoic acid (1.0g), alpha-cyano-3-phenoxybenzyl bromide (1.9g) and potassium carbonate (1.0g) in anhydrous acetone (40ml) was stirred at room temperature for 4 hours. Water was added to the reaction mixture and the product extracted with ether, the ethereal extracts washed with water (X2) and dried over magnesium sulphate. Evaporation of the solvent gave a crude product which was purified by chromatography on silica gel using 3% acetone in 60°-80° C. petroleum ether as eluent to give the desired ester. R.I. nD20 1.5343.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04042710 |
| Source dataset | uspto-grants-1977_08 |
| ORD ID | ord-36732275e3d3415d9b09f797ba180afb |
| Source note | uspto-grants-1977_08 |