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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873132Generated: October 31, 2026

(4-Chloro-3-(trifluoromethyl)phenoxy)benzaldehyde → 1-Chloro-2-(trifluoromethyl)-4-(4-vinylphenoxy)benzene

https://huagongshe.com/reaction/873132

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Chloro-3-(trifluoromethyl)phenoxy)benzaldehydeHCID 86676377—
ReactantButyllithiumHCID 178418339—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventTetrahydrofuranHCID 8028—
Product1-Chloro-2-(trifluoromethyl)-4-(4-vinylphenoxy)benzeneHCID 6682583774.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of methyl(triphenyl)phosphonium bromide (5.56 g, 15.57 mmol) in anhydrous tetrahydrofuran (THF) (50 mL) was added BuLi (9.5 ml, 15.20 mmol) dropwise at 0° C. The reaction mixture was turned to clear and stirred for 15 min at 0° C., then a solution of -{[4-chloro-3-(trifluoromethyl)phenyl]oxy}benzaldehyde (4.07 g, 13.54 mmol) in THF (10 mL) was added. The reaction mixture was warmed to rt and stirred for 1 h, quenched by sat. NH4Cl, and then concentrated. The residue was dissolved in ethyl acetate (100 mL), washed with water, and brine, dried over anhydrous sodium sulfate, concentrated. Purification via ISCO afforded the title compound (3.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975400B2
Source datasetuspto-grants-2015_03
ORD IDord-c07d1c13a6c84b7385b89a4e3d4b19a6
Source noteuspto-grants-2015_03