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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloromethyl Methyl Ether | HCID 7864 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Bromo-4,6-di-tert-butylphenol | HCID 519822 | — |
| Reactant | Ether hydrochloride | HCID 10953452 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Bromo-3,5-bis(1,1-dimethylethyl)-2-(methoxymethoxy)benzene | HCID 22592638 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06849658B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-fb17e6201ae24177862d7baad47c5a19 |
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| Source note | uspto-grants-2005_02 |
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