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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289400Generated: October 31, 2026

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

https://huagongshe.com/reaction/1289400

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. A 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 numberUS05750213
Source datasetuspto-grants-1998_05
ORD IDord-85cee6e71a894c82af82dac423c4e48f
Source noteuspto-grants-1998_05