HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → Benzoic acid, 2,3,4,5-tetrachloro-6-cyano-, methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Methyl Ethyl Ketone | HCID 6569 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | 2,3,4,5-Tetrachloro-6-cyanobenzoic acid | HCID 14047705 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzoic acid, 2,3,4,5-tetrachloro-6-cyano-, methyl ester | HCID 79319 | — |
Reaction Steps
12.9 g of the potassium salt of 3,4,5,6-tetrachloro-2-cyanobenzoic acid are heated for 20 hours under reflux in a mixture of 30 ml of water, 60 ml of methyl ethyl ketone and 11.4 g of methyl iodide. The aqueous phase is separated and the organic phase is concentrated by evaporation. Recrystallisation of the crude product (which contains only a small amount of impurities according to analysis by thin-layer chromatography) from ethanol affords 7.5 g of pure methyl 3,4,5,6-tetrachloro-2-cyanobenzoate with a melting point of 83°-84° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04978768 |
| Source dataset | uspto-grants-1990_12 |
| ORD ID | ord-69a0ccf906b7406885ef849bfa64b83c |
| Source note | uspto-grants-1990_12 |