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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699431Generated: November 3, 2026

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

https://huagongshe.com/reaction/1699431

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 (100%) of the expected compound are collected in the form of an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06346546B1
Source datasetuspto-grants-2002_02
ORD IDord-14946a640b6e484aa929213934992a4d
Source noteuspto-grants-2002_02