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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603632Generated: November 1, 2026

Anisole → Benzene, 1-(6-bromohexyl)-4-methoxy-

https://huagongshe.com/reaction/1603632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnisoleHCID 7519—
ReactantTriethylsilaneHCID 12052—
Reactant6-Bromohexanoyl chlorideHCID 89848—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
ProductBenzene, 1-(6-bromohexyl)-4-methoxy-HCID 1058817133.8%

Reaction Steps

A solution of 6-bromohexanoyl chloride (50 g, 0.2 mol) in dry dichloromethane (40 ml) was added dropwise over 5 minutes to a suspension of aluminium chloride (31 g, 0.2 mol) in dry dichloromethane (100 ml), keeping the temperature between 20-23° C. The mixture was stirred for 30 minutes at room temperature to give a yellow solution. Anisole (23 g, 0.2 mol) in dry dichloromethane (30 ml) was added and stirred for 20 hours at room temperature. Triethylsilane (59.9 g, 0.515 mol) was added over 10 minutes, maintaining the temperature between 25° C.-35° C. The solution was stirred for 60 minutes at room temperature and poured onto ice/water (200 g). The organic layer was washed with brine and water until the pH of the solution was neutral. Drying (MgSO4) and evaporation under reduced pressure gave a yellow oil which was distilled under reduced pressure at 90-110° C./0.5 mbar. Produce containing fractions were combined and purified by flash chromatography on silica gel using hexane as eluant to give a colourless oil (18.33 g, 33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990102
Source datasetuspto-grants-1999_11
ORD IDord-ce3f834a661748b7bcee41cc14f43abe
Source noteuspto-grants-1999_11