HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → trans 2-Bromo-6-chlorobenzyl 2-(2,2-dichlorovinyl)-3,3-dimethylcyclopropane carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Trans-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropane carboxylic acid | HCID 41539 | — |
| Reactant | 2-Bromo-6-chlorobenzyl bromide | HCID 2756872 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | trans 2-Bromo-6-chlorobenzyl 2-(2,2-dichlorovinyl)-3,3-dimethylcyclopropane carboxylate | HCID 131712138 | 98% |
Reaction Steps
1 cis/trans 2-(2,2-dichlorovinyl)-3,3-dimethylcyclopropane carboxylic acid (2.3 g), 2-bromo-6-chlorobenzylbromide (2.85 g) and potassium carbonate (1.6 g) were stirred together in acetone (30 ml) under reflux for 6 hours. The reaction mixture was cooled, diluted with water, and extracted three times with 50 ml portions of diethyl ether. The combined ether extracts were washed with water and with aqueous sodium bicarbonate solution (three times), dried over magnesium sulphate and evaporated to give the orange title product (4. g, 98%) m.p. 61°-67° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04259349 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-86a8a7b9788b4e6e9447e9f7d06881be |
| Source note | uspto-grants-1981_03 |