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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261841Generated: October 25, 2026

Pyridine → alpha-Trifluoromethyl-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutanoate

https://huagongshe.com/reaction/261841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-(4-Chlorophenyl)-3-methylbutanoyl chlorideHCID 4178001—
Reactant2,2,2-Trifluoro-1-(3-phenoxyphenyl)ethan-1-olHCID 14270571—
SolventTolueneHCID 1140—
Productalpha-Trifluoromethyl-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutanoateHCID 5381839098.3%

Reaction Steps

This compound was prepared in the manner of Example II, using 5.3 g of 2-(4-chlorophenyl)-3-methylbutanoyl chloride, whose preparation is described in Agr. Biol. Chem., 38, 881 (1974), together with J. Kagaku To Seibutsu, 14, 427 (1976), 4.6 g of α-trifluoromethyl-3-phenoxybenzyl alcohol, and 1.5 g of pyridine in 50 ml of toluene. Volatiles were removed from the crude reaction product at 100° C./0.02 mm through a short path Kugelrohr distillation system to give as a residue 7.8 g of α-trifluoromethyl-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutanoate. The ir spectrum was consistent with the assigned structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04152455
Source datasetuspto-grants-1979_05
ORD IDord-2168c1c5860e41bcbe412bf4e1bd93fc
Source noteuspto-grants-1979_05