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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1447439Generated: October 29, 2026

Sodium Hydroxide → HCID 54111873, compound

https://huagongshe.com/reaction/1447439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 54388179HCID 54388179—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 54111873HCID 5411187368.3%

Reaction Steps

30.8 g (0.085 mol) of 2,2-dimethyl-3-(2-chloro-2-(4-trifluoromethoxy-phenyl)-vinyl)-cyclopropanecarboxylic acid ethyl ester were dissolved in 100 ml of ethanol, a solution of 4 g (0.1 mol) of sodium hydroxide in 100 ml of water was then added and the mixture was heated to the reflux temperature for 4 hours, while stirring. The ethanol was then distilled off under a waterpump vacuum, the residue was taken up in 300 ml of warm water and the mixture was extracted once with 300 ml of methylene chloride. The aqueous phase was separated off, acidified with concentrated hydrochloric acid and then extracted with 2 times 300 ml of methylene chloride. The organic phase was then separated off and dried over magnesium sulphate and the solvent was distilled off under a waterpump vaccum. Last residues of solvent were removed by brief incipient distillation under 2 mm Hg at a bath temperature of 60° C. 19.4 g (68.3% of theory) of 2,2-dimethyl-3-(2-chloro-2-(4-trifluoromethoxy-phenyl)-vinyl)-cyclopropanecarboxylic acid (cis and trans, E and Z isomer mixture) were then obtained as a very viscous yellow oil. The structure was confirmed by the 1H-NMR spectrum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04316913
Source datasetuspto-grants-1982_02
ORD IDord-1b4066bddc9d4672851c11b5077d25cd
Source noteuspto-grants-1982_02