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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 750936Generated: November 3, 2026

4-Bromoanisole → 1-(4-Bromobutyl)-4-methoxybenzene

https://huagongshe.com/reaction/750936

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromoanisoleHCID 7730—
Reactant1,4-DibromobutaneHCID 8056—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium ChlorideHCID 433294—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product1-(4-Bromobutyl)-4-methoxybenzeneHCID 578191—

Reaction Steps

After starting the reaction by adding 5.00 ml 4-bromoanisole to a mixture of 4.86 g (0.20 mol) magnesium turnings and 100 ml THF, 20.00 ml 4-bromoanisole (total: 25.0 ml (37.4 g; 0.20 mol) were added at a pace sufficient to maintain reflux temperature. The reaction mixture was heated to reflux for additional 3 h, cooled to r.t. and dropped at 0° C. within 1 h to a stirred solution prepared by mixing 129.6 g (71.6 ml, 0.60 mol) 1,4-dibromo-butane in 200 ml THF with a freshly prepared solution of 0.17 g (4.0 mmol) LiCl and 0.267 g (2.0 mmol) Cu(II)Cl2 in 20 ml THF. Stirring was continued for 12 h at r.t. followed by the addition of 100 ml of a 20% ammonium chloride solution and 200 ml ethyl acetate. The water phase was extracted twice with 50 ml ethyl acetate, all organic phases were combined, dried over sodium sulphate and evaporated. The resulting oil was fractionated by vacuum distillation. Yield: 27.7 g (57%), b.p. 112-115° C./0.15 mbar.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07405231B2
Source datasetuspto-grants-2008_07
ORD IDord-fe397c1be7974c76a3d96e0f1af2f3ff
Source noteuspto-grants-2008_07