HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716459Generated: October 30, 2026
Acetonitrile → 1-Bromo-4-methoxy-2-methylbenzene
https://huagongshe.com/reaction/716459
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 3-Methoxytoluene | HCID 7530 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Product | 1-Bromo-4-methoxy-2-methylbenzene | HCID 117915 | 86% |
Reaction Steps
To a solution of 122 g (1.0 mol) of 1-methoxy-3-methylbenzene in 1 L of acetonitrile 178 g (1.0 mol) of NBS was added in small portions by vigorous stirring for 1 h at 10° C. The reaction mixture was stirred at ambient temperature overnight and then evaporated to dryness. The residue was dissolved in 1 L of n-hexane and filtered through glass frit (G2). The precipitate was additionally washed by 2×150 ml of n-hexane. The combined filtrate was evaporated to dryness to give 173 g (86%) of 1-bromo-4-methoxy-2-methylbenzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187583B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-47b6525a07c542d48306fdb333932ac7 |
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| Source note | uspto-grants-2015_11 |
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