Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 972009Generated: October 26, 2026

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

https://huagongshe.com/reaction/972009

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., 31, 1148 (1967), 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 numberUS04162366
Source datasetuspto-grants-1979_07
ORD IDord-352c8a90814d44b7bf510ec885d5ce64
Source noteuspto-grants-1979_07