HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Cyanide → Cypothrin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 3-Phenoxybenzaldehyde | HCID 38284 | — |
| Reactant | 3,3-Dimethylspiro(cyclopropane-1,1'-(1H)indene)-2-carbonyl chloride | HCID 108458 | — |
| Solvent | Water | HCID 962 | — |
| Product | Cypothrin | HCID 65491 | — |
Reaction Steps
A mixture of 0.05 gram-mole of m-phenoxybenzaldehyde and 0.05 gram-mole of 3,3-dimethylspiro[cyclopropane-1,1'-indene]-2-carboxylic acid chloride is added slowly, portionwise, to a solution of 0.075 gram-mole of potassium cyanide in 100 ml of water at 5° C. the mixture is stirred for 1.5 hours at 5° and then extracted with three 50--ml portions of ether. The extracts are washed with 10% hydrochloric acid solution, saturated sodium bicarbonate solution, and water and then dried over sodium sulfate. Removal of the ether under vacuum leaves α-cyano-m-phenoxybenzyl 3,3-dimethylspiro[cyclopropane-1,1'-indene]-2-carboxylate as a yellow-brown oil which is a useful insecticide as taught in U.S. Pat. No. 3,966,959 (1976).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04108904 |
| Source dataset | uspto-grants-1978_08 |
| ORD ID | ord-dc7f9291608b4069bcee522a393ee05e |
| Source note | uspto-grants-1978_08 |