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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1861487Generated: November 1, 2026

Water → 4-Bromo-3-isopropylanisole

https://huagongshe.com/reaction/1861487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
Reactant1-Isopropyl-3-methoxy-benzeneHCID 10931606—
SolventCarbon TetrachlorideHCID 5943—
Product4-Bromo-3-isopropylanisoleHCID 1174640681.3%

Reaction Steps

A mixture of 1-isopropyl-3-methoxy-benzene (Intermediate 142, 3.50 g, 23.3 mmols), molecular sieves, and silica gel in 150 mL CCl4 was treated with N-bromosuccinimide (4.98 g, 28.0 mmols) at 35° C. for 18 hours. An additional portion of N-bromosuccinimide (830.0 mg, 4.46 mmols) was added and stirring continued for 6 hours. The mixture was cooled to room temperature, H2O was added, and the mixture was filtered to remove the solids. The mixture was extracted with E2O and the combined organic layers were washed with 10% aqueous HCl, H2O, saturated aqueous NaHCO3, and saturated NaCl before being dried (MgSO4) and concentrated under reduced pressure. Column chromatography (2.5% EtOAc-hexanes) afforded 4.34 g (81%) of the title compound as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06531599B2
Source datasetuspto-grants-2003_03
ORD IDord-eb57635d2e794cf3b76a71a8b6e7ab38
Source noteuspto-grants-2003_03