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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631171Generated: October 30, 2026

Chloromethyl Methyl Ether → 1-BROMO-4-(METHOXYMETHOXY)-2-METHYLBENZENE

https://huagongshe.com/reaction/631171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantSodium hydrideHCID 24758—
Reactant4-Bromo-m-cresolHCID 72857—
SolventDimethylformamideHCID 6228—
Product1-BROMO-4-(METHOXYMETHOXY)-2-METHYLBENZENEHCID 11557681—

Reaction Steps

To a solution of 4-bromo-3-methylphenol (6) (1.0 equiv.) in DMF (0.5 M) at 0° C. was added portionwise 60% wt NaH (1.5 equiv.). The addition was controlled such that internal reaction temperature never went above 10° C. The reaction was stirred at room temperature for 45 minutes, then a solution of chloro(methoxy)methane (1.2 equiv.) in DMF (3M) was added dropwise via additional funnel. The reaction was stirred at room temperature for 3.5 hours, and then quenched by pouring into ice. The resulting mixture was stirred at room temperature for 1 hour. Ether was added, and the two layers were separated. The aqueous layer was extracted (1×) with ether. The combined organic layers were washed with water (2×), brine, dried over MgSO4, and concentrated to give 1-bromo-4-(methoxymethoxy)-2-methylbenzene (7) as a colorless oil. The crude material was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09320748B2
Source datasetuspto-grants-2016_04
ORD IDord-67248927fd45401cb11a6c84f35a1504
Source noteuspto-grants-2016_04