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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376862Generated: November 1, 2026

Chloromethyl Methyl Ether → 1-Bromo-3,5-bis(1,1-dimethylethyl)-2-(methoxymethoxy)benzene

https://huagongshe.com/reaction/1376862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Bromo-4,6-di-tert-butylphenolHCID 519822—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDichloromethaneHCID 6344—
Product1-Bromo-3,5-bis(1,1-dimethylethyl)-2-(methoxymethoxy)benzeneHCID 2259263895.4%

Reaction Conditions

Temperature45 °C

Reaction Steps

To a solution of 2-bromo-4,6-di-t-butylphenol (Compound D 2.54 g, 8.88 mmol) and catalytic amount of Bu4NI in 20 ml of dry CH2Cl2 at 0° C. was added diisopropylethylamine (9.51 ml, 53 mmol), followed by methoxymethyl chloride (2.02 ml, 26.6 mmol). The reaction mixture was heated to 45° C. for 12 hours. The reaction mixture was then washed with 10% citric acid, then NaHCO3 (sat.), brine, and dried over MgSO4. After filtration and removal of the solvent under reduced pressure, the residue was purified by column chromatography (pure hexane) to yield the title compound (2.79 g) as a colorless oil. 1H NMR δ 7.40 (d, J=2.44 Hz, 1H), 7.30 (d, J=2.4 Hz, 1H), 5.22 (s, 2H), 3.70 (s, 3H), 1.43 (s, 9H), 1.29 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663357
Source datasetuspto-grants-1997_09
ORD IDord-6fcc195d42f04a7cb595ee7bbbd5b268
Source noteuspto-grants-1997_09