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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061434Generated: November 3, 2026

Methoxymethyl-triphenylphosphonium chloride → 4-Chloro-2-(1-cyclopropyl-2-methoxyvinyl)-3-methylpyridine

https://huagongshe.com/reaction/1061434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethoxymethyl-triphenylphosphonium chlorideHCID 2723798—
Reactant(4-Chloro-3-methyl-2-pyridyl)cyclopropylketoneHCID 66980317—
ReactantHCID 178506676HCID 178506676—
SolventDiethyl EtherHCID 3283—
Product4-Chloro-2-(1-cyclopropyl-2-methoxyvinyl)-3-methylpyridineHCID 6698022448.2%

Reaction Steps

5.54 g of (methoxymethyl) triphenyl phosphonium chloride is suspended in 53 ml of anhydrous ether and 18.4 ml of phenyllithium (0.88 M) was dropped thereto and the resulting mixture was stirred at a room temperature for 15 minutes. 35 ml of ether solution of 3.01 g of (4-chloro-3-methyl-2-pyridyl)cyclopropylketone (X) was dropped thereto and the resulting mixture was stirred at a room temperature for 2 hours. The resulting residue was separated by filtering and washed with ether, and thereafter, the ether filtrate and ether used for washing were collected together and the collected solution was washed with water, and thereafter, dried over anhydrous sodium sulfate and the solvent was distilled off under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent; hexane:ethyl acetate=4:1) to obtain 1.66 g of 2-(4-chloro-3-methyl-2-pyridyl)-2-cyclopropyl-1-methoxyethene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06525066B2
Source datasetuspto-grants-2003_02
ORD IDord-e61ff8f32b97474db61a3560936f9e6e
Source noteuspto-grants-2003_02