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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22996Generated: October 29, 2026

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

https://huagongshe.com/reaction/22996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantSodium hydrideHCID 24758—
Reactant2-Bromo-4,6-di-tert-butylphenolHCID 519822—
ReactantEther hydrochlorideHCID 10953452—
SolventDimethylformamideHCID 6228—
Product1-Bromo-3,5-bis(1,1-dimethylethyl)-2-(methoxymethoxy)benzeneHCID 22592638—

Reaction Conditions

Temperature7.5 °C

Reaction Steps

40.00 g (140.2 mmol) of 2,4-di-tert-butyl-6-bromophenol and 400 ml of DMF are introduced into a one liter three-necked flask. The solution obtained is cooled to 5-10° C., 4.70 g of sodium hydride are added and the mixture is stirred at 10° C. for 30 minutes. 11.7 ml (154.0 mmol) of chloromethyl methyl ether are then added dropwise and the reaction mixture is stirred for one hour at room temperature. The reaction mixture is poured into a 1N HCl/ethyl ether mixture and extracted with ethyl ether and the organic phase is separated by settling, dried over magnesium sulphate and evaporated. 46.00 g (130%) of the expected compound are collected in the form of an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06849658B2
Source datasetuspto-grants-2005_02
ORD IDord-fb17e6201ae24177862d7baad47c5a19
Source noteuspto-grants-2005_02