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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418763Generated: November 3, 2026

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

https://huagongshe.com/reaction/1418763

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 methylene chloride 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 (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 (3) as an oil; 1HNMR (CDCl3) δ 1.2 (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 numberUS05883294
Source datasetuspto-grants-1999_03
ORD IDord-82b80b1591884613b47e0cf1125ecb41
Source noteuspto-grants-1999_03