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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51807Generated: October 25, 2026

Water → 4-Bromo-3-isopropylanisole

https://huagongshe.com/reaction/51807

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 numberUS06713647B2
Source datasetuspto-grants-2004_03
ORD IDord-d92859c607754ef08138ecd8c685a770
Source noteuspto-grants-2004_03