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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768035Generated: October 31, 2026

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

https://huagongshe.com/reaction/1768035

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 Grignard 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 numberUS07235574B2
Source datasetuspto-grants-2007_06
ORD IDord-bf724c81354f4028bb494a566e952a8e
Source noteuspto-grants-2007_06