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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606703Generated: November 2, 2026

Methoxymethyl-triphenylphosphonium chloride → 2,6-Diisopropyl-4-bromo-beta-methoxystyrene

https://huagongshe.com/reaction/606703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethoxymethyl-triphenylphosphonium chlorideHCID 2723798—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant2,6-Diisopropyl-4-bromobenzaldehydeHCID 57437668—
SolventTetrahydrofuranHCID 8028—
Product2,6-Diisopropyl-4-bromo-beta-methoxystyreneHCID 6681356678.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

Methoxymethyl triphenylphosphonium chloride (18.68 g, 54.5 mmol) was suspended in 200 mL of THF at −78° C. Lithium hexamethyldisilazide (1.0 M in THF, 50 mL) was added dropwise. The resulting mixture was warmed up to 0° C. with stirring. After cooling the solution to −78° C., 2,6-diisopropyl-4-bromobenzaldehyde (11.5 g, 42.7 mmol) in 20 mL of THF was added dropwise. The mixture was slowly warmed up to room temperature and continually stirred overnight. After regular work up, the crude product was distilled at 165° C. under vacuum to afford 2,6-diisopropyl-4-bromo-β-methoxystyrene (10 g). This product was dissolved in 20 mL of dioxane and 100 mL of 18% HCl solution and refluxed at 100° C. for 6 h. After regular work up, the crude product was distilled at 160° C. under vacuum to afford 2,6-diisopropyl-4-bromophenylacetaldehyde (7.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915415B2
Source datasetuspto-grants-2011_03
ORD IDord-3e151b76e5b242a384b9bbfac0c64e72
Source noteuspto-grants-2011_03