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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloromethyl Methyl Ether | HCID 7864 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Bromo-m-cresol | HCID 72857 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-BROMO-4-(METHOXYMETHOXY)-2-METHYLBENZENE | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09320748B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-67248927fd45401cb11a6c84f35a1504 |
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| Source note | uspto-grants-2016_04 |
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