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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2194554Generated: October 27, 2026

tert-Butyl methyl ether → 4-Bromo-2-(2-methylallyl)phenol

https://huagongshe.com/reaction/2194554

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl methyl etherHCID 15413—
Reactant1-Bromo-4-[(2-methylprop-2-en-1-yl)oxy]benzeneHCID 235995—
SolventDimethylformamideHCID 6228—
Product4-Bromo-2-(2-methylallyl)phenolHCID 8676172465%

Reaction Steps

A solution of 1-bromo-4-(2-methylallyloxy)benzene (6) (1.0 g, 4.4 mmol) in DMF (8 mL) was heated in a microwave reactor at 190° C. for 2 h. After cooling to room temperature, the reaction mixture was diluted with methyl tert-butyl ether (50 mL), and washed with H2O (25 mL), brine (25 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography (silica gel, eluting with 5% ethyl acetate in hexanes) to give the title compound (7) (0.7 g, 65%) as a liquid. 1H NMR (CDCl3, 400 MHz) δ 7.27-7.25 (m, 2H), 6.72 (d, J=8.4 Hz, 1H), 4.95 (s, 1H), 4.86 (s, 1H), 3.34 (s, 2H), 1.74 (s, 3H); MS (ESI, M+H+) C10H12BrO, calcd. 227.1. found 227.0, 229.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08334292B1
Source datasetuspto-grants-2012_12
ORD IDord-6395a0d0876e4fa5bf37d43d831eb54b
Source noteuspto-grants-2012_12