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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1872419Generated: November 3, 2026

18-Crown-6 → 4-Bromo-2-isopropyl-1-methoxybenzene

https://huagongshe.com/reaction/1872419

Reaction equation

Participants

RoleNameHCIDCharge
Reactant18-Crown-6HCID 28557—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantPotassium BromideHCID 253877—
Reactant2-IsopropylanisoleHCID 270623—
SolventDichloromethaneHCID 6344—
Product4-Bromo-2-isopropyl-1-methoxybenzeneHCID 1469879472%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of potassium bromide (18.8 g, 157.7 mmol) in 400 mL of CH2Cl2 at 0° C. were added 18-Crown-6 (2.08 g, 7.88 mmol), 3-chloroperoxy benzoic acid (27.2 g, 157.7 mmol) and 2-isopropylanisole (a compound of Formula 1 from Example 1) (12.0 g, 78.8 mmol). After stirring for 3 hours at 0° C., the reaction mixture was poured into ice water (500 mL), and stirred for 30 minutes. The organic layer was separated, washed with saturated NaHCO3 solution (400 mL), followed by water (300 mL), and dried (MgSO4). The solvent was evaporated to give an oil, which was purified by flash column chromatography (silica gel, 98:2 hexane/ethylacetate) to give 13 g (56.7 mmol, 72%) of 4-bromo-2-isopropylanisole (a compound of Formula 3) as an oil; 1HNMR (CDCl3) δ1.2 (d, 6H), 3.3 (heptet, 1H), 6.7 (d, 1H), 6.84 (d, 1H), 7.29 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06107517
Source datasetuspto-grants-2000_08
ORD IDord-1ac1ec4cae024a32a755ab183eff0092
Source noteuspto-grants-2000_08