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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726491Generated: October 30, 2026

Methoxymethyl-triphenylphosphonium chloride → 1-(2,3-Difluorophenyl)-4-methoxymethylene cyclohexane

https://huagongshe.com/reaction/726491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethoxymethyl-triphenylphosphonium chlorideHCID 2723798—
Reactant4-(2,3-Difluorophenyl)cyclohexanoneHCID 18920872—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDiethyl EtherHCID 3283—
Product1-(2,3-Difluorophenyl)-4-methoxymethylene cyclohexaneHCID 1892085989.8%

Reaction Steps

First, 27.4 g of (methoxymethyl)triphenylphosphonium chloride, 9 g of potassium t-butoxide, and 225 ml of dry ether were placed in a 500 ml flask whose content was replaced with argon. The mixture was stirred for 30 minutes under ice water cooling. Then, 50 ml of an ether solution containing 16.8 g of 4-(2,3-difluorophenyl)cyclohexanone was added dropwise to the reaction mixture. The reaction mixture was stirred under ice water cooling for 30 minutes and at room temperature for 8 hours. Thereafter, a precipitate was filtered out. The filtrate was washed with water and dried over anhydrous sodium sulfate. The solvent was distilled away. Thereafter, the residue was purified by silica gel column chromatography (eluent: toluene/hexane=1/4) to obtain 17.1 g of 1-(2,3-difluorophenyl)-4-methoxymethylene cyclohexane (Y: 89.7%). The compound thus obtained had a purity of 99.2% by GC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05709911
Source datasetuspto-grants-1998_01
ORD IDord-d8f18c606b4044af925cb599365ed928
Source noteuspto-grants-1998_01