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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894546Generated: October 29, 2026

Water → HCID 70527796, compound

https://huagongshe.com/reaction/894546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CyanideHCID 8929—
Reactant4-Fluoro-3-phenoxybenzaldehydeHCID 110068—
ReactantHCID 20343288HCID 20343288—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
ProductHCID 70527796HCID 7052779680.1%

Reaction Steps

8.64 g (0.04 mol) of 3-phenoxy-4-fluoro-benzaldehyde and 11.22 g (0.04 mol) of α-isopropyl-4-trifluoromethoxy-phenyl-acetic acid chloride were together added dropwise to a mixture of 3 g of sodium cyanide, 4.7 ml of water, 200 ml of n-hexane and 1 g of tetrabutylammonium bromide at 20°-25° C., while stirring, and the mixture was then stirred at 20°-25° C. for 4 hours. 300 ml of toluene were then added to the reaction mixture and the mixture was extracted by shaking twice 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. 15.6 g (80.1% of theory) of α-isopropyl-4-trifluoromethoxy-phenylacetic acid 3-phenoxy-4-fluoro-α-cyanobenzyl ester were obtained as a yellow oil with the refractive index nD29 : 1.5185.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04284643
Source datasetuspto-grants-1981_08
ORD IDord-96f526f8cdc34bcab6ebb062fdd3fb97
Source noteuspto-grants-1981_08