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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979818Generated: November 1, 2026

Water → HCID 67991653, compound

https://huagongshe.com/reaction/1979818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CyanideHCID 8929—
Reactant4-Fluoro-3-phenoxybenzaldehydeHCID 110068—
ReactantHCID 131713965HCID 131713965—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
ProductHCID 67991653HCID 67991653—

Reaction Steps

6.36 g (0.017 mole) of trans-3-(1,2,2-trichloro-2-(4-chloro-phenyl)-ethyl)-2,2-dimethyl-cyclo-propane-1-carboxylic acid chloride and 3,67 g (0.017 mole) of 3-phenoxy-4-fluoro-benzaldehyde were together added dropwise to a mixture of 1.13 g of sodium cyanide, 1.7 ml of water, 100 ml of n-hexane and 0.6 g of tetrabutylammonium bromide at 20°-25° C., whilst stirring, and the mixture was then stirred at 20°-25° C. for 4 hours. 300 ml of toluene were subsequently added to the reaction mixture, and the mixture was extracted twice by shaking with 300 ml of water each time. The organic phase was separated off and dried over magnesium sulphate, and the solvent was distilled off under a waterpump vacuum. Last residues of solvent were removed by brief incipient distillation at a bath temperature of 60° C./1 mm Hg. 8.5 g (86% of theory) of trans-3-(1,2,2-trichloro-2-(4-chloro-phenyl)-ethyl)-ethyl)-2,2-dimethyl-cyclopropane-1-carboxylic acid α-cyano-3-phenoxy-4-fluorobenzyl ester were obtained as a viscous oil. ##STR35##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04482731
Source datasetuspto-grants-1984_11
ORD IDord-c4fe2437e2f14ab69437906e03ef6bce
Source noteuspto-grants-1984_11