HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059328Generated: October 25, 2026
Sodium Cyanide → alpha-Cypermethrin 1-Epimeric Mixture
https://huagongshe.com/reaction/2059328
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 3-Phenoxybenzaldehyde | HCID 38284 | — |
| Reactant | cis-3-(2,2-Dichlorovinyl)-2,2-dimethylcyclopropylcarbonyl chloride | HCID 12617358 | — |
| Reactant | 3-(Cyanohexylamino)propanesulfonic acid | HCID 86738320 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | alpha-Cypermethrin 1-Epimeric Mixture | HCID 9801977 | — |
Reaction Steps
A stirred mixture of sodium cyanide (18.0 g, 0.36 mole) and 3-(cyanohexylamino)propanesulfonic acid (1.34 g, 0.006 mole) in 300 ml of water was warmed to 40°. During a one hour period, maintaining a reaction temperature of about 40°, a solution of cis-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropanecarbonyl chloride (71.7 g, 0.315 mole) and 3-phenoxybenzaldehyde (61.9 g, 0.3 mole) in 262.2 g of n-heptane was added. The mixture was then stirred at 40° for one additional hour, after which it was washed with an aqueous solution containing 20% sodium carbonate and then with water. The organic phase was separated from the mixture and the solvent removed by distillation under reduced pressure to give α-cyano-3-phenoxybenzyl cis-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropanecarboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04322535 |
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| Source dataset | uspto-grants-1982_03 |
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| ORD ID | ord-343e4a549518433ab27d33aa24c2fdb3 |
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| Source note | uspto-grants-1982_03 |
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