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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 31560Generated: October 31, 2026

Methoxymethyl-triphenylphosphonium chloride → 2-Isopropyl-6-(4-isopropyl-2-(2-methoxyvinyl)phenyl)naphthalene

https://huagongshe.com/reaction/31560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethoxymethyl-triphenylphosphonium chlorideHCID 2723798—
Reactant5-Isopropyl-2-(6-isopropyl-2-naphthyl)benzaldehydeHCID 86226184—
ReactantHCID 178418922HCID 178418922—
SolventTetrahydrofuranHCID 8028—
Product2-Isopropyl-6-(4-isopropyl-2-(2-methoxyvinyl)phenyl)naphthaleneHCID 6883660590%

Reaction Steps

Under an atmospheric argon gas flow, 5-isopropyl-2-(6-isopropyl-2-naphthyl)benzaldehyde in an amount of 4.4 g (14 mmol), (methoxymethyl)triphenylphosphoniumchloride in an amount of 5.1 g (15 mmol), t-butoxypotassium in an amount of 1.7 g (15 mmol) and desiccated tetrahydrofuran in an amount of 100 milliliter were placed into a three-necked flask equipped with a cooling pipe and having a capacity of 500 milliliter, and the resultant solution was stirred under heating at the room temperature for one night. After the reaction terminated, adding water in an amount of 100 milliliter into the reacted solution, an organic layer was separated, followed by drying with the use of magnesium sulfate. After removing the solvent by distillation by means of a rotary evaporator, the resultant crude product was refined by means of column chromatography (silicagel, hexane/dichloromethane=10/90), and as a result, 4.3 g of an aimed compound (white crystal) was obtained (yield: 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07425653B2
Source datasetuspto-grants-2008_09
ORD IDord-5acbbd5a610e460b8b702bf89d8d63c3
Source noteuspto-grants-2008_09