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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848763Generated: November 1, 2026

Hydrochloric Acid → HCID 54304438, compound

https://huagongshe.com/reaction/848763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
Reactant3-Phenoxybenzyl alcoholHCID 26295—
ReactantHCID 53757527HCID 53757527—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 54304438HCID 5430443887.7%

Reaction Steps

5.2 g (0.026 mol) of 3-phenoxy-benzyl alcohol and 7 g (0.026 mol) of 2,2-dimethyl-3-(3,3,3-trifluoro-2-ethoxy-prop-1-enyl)-cyclopropanecarboxylic acid chloride were dissolved in 100 ml of anhydrous toluene, and 2.5 g of pyridine, dissolved in 20 ml of anhydrous toluene, were added dropwise at 20°-25° C., while stirring. Stirring was then continued at 25°-35° C. for 3 hours. The reaction mixture was poured into 150 ml of water, to which 10 ml of concentrated hydrochloric acid were added, and the organic phase was separated off and washed again with 100 ml of water. The toluene phase was then dried over sodium sulphate and the solvent was distilled off under a water-pump vacuum. Last residues of solvent were removed by brief incipient distillation at a bath temperature of 60° C./1 mm Hg. 9.9 g (87.7% of theory) of 2,2-dimethyl-3-(3,3,3-trifluoro-2-ethoxy-prop-1-enyl)-cyclopropanecarboxylic acid 3-phenoxybenzyl ester were obtained as a yellow oil with the refractive index nD25 : 1.5130.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04297366
Source datasetuspto-grants-1981_10
ORD IDord-c62a85f66e1a4912a0bd4ee30450ff53
Source noteuspto-grants-1981_10