HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783351Generated: October 31, 2026
N-bromobutanimide → 4-Bromo-2-methoxy-6-methylaniline
https://huagongshe.com/reaction/1783351
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Methoxy-6-methylaniline | HCID 459249 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Bromo-2-methoxy-6-methylaniline | HCID 10680218 | 26% |
Reaction Steps
To 2-methoxy-6-methyl-phenylamine (10.0 g) dissolved in acetonitrile (200 mL) was added N-bromosuccinimide (14.3 g) and the reaction mixture was heated to 145° C. for 15 minutes in a sealed microwave process vessel. The crude mixture was filtered through Celite, diluted with diethyl ether (200 mL) and washed with sodium hydroxide (2 M, 2×100 mL) and brine (1×100 mL). The organic phase was dried over magnesium sulfate, concentrated in vacuo and purified by flash chromatography to furnish 3.4 g (26%) of the title compound as a black solid. 1H NMR (500 MHz, DMSO-d6): 2.06 (s, 3H), 3.77 (s, 3H), 4.55 (s, 2H), 6.78 (d, 1H), 6.82 (d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07501414B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-65f6ee47b2704f1a9cc633e1faf63866 |
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| Source note | uspto-grants-2009_03 |
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