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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 725661Generated: October 26, 2026

Ammonium Chloride → 4-Methoxy-3-(4-methoxy-2-butenyl)-bromobenzene

https://huagongshe.com/reaction/725661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant5-Bromo-2-methoxybenzaldehydeHCID 90684—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant(3-Methoxypropyl)triphenylphosphonium bromideHCID 21458797—
SolventTetrahydrofuranHCID 8028—
Product4-Methoxy-3-(4-methoxy-2-butenyl)-bromobenzeneHCID 54142774—

Reaction Conditions

Temperature0 °C

Reaction Steps

251.1 g of 3-methoxypropyltriphenylphosphonium bromide are added to a solution, stirred at 5° C., of 110.8 g of sodium bis(trimethylsilyl)amide in 1200 ml of tetrahydrofuran. The reaction mixture is further stirred for 45 minutes at 0° C. and then a solution of 100 g of 5-bromo-o-anisaldehyde in 1000 ml of tetrahydrofuran is added dropwise thereto. The reaction mixture is stirred for a further 1 hour at 0° C. Then, at 0° C., 1 liter of a saturated ammonium chloride solution is added dropwise. After concentration, the residue is extracted 4 times with ethyl acetate. The organic phases are washed with water and saturated sodium chloride solution and concentrated by evaporation. The residue is purified by FC (500 g of silica gel, hexane/ethyl acetate=5:1). Distillation under a high vacuum yields the title compound: Rf (hexane/ethyl acetate=4:1)=0.61.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05705658
Source datasetuspto-grants-1998_01
ORD IDord-72a0548e42864fe0a0bf2cb7d4be73f2
Source noteuspto-grants-1998_01