HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678709Generated: October 25, 2026
N-bromobutanimide → 1-(Bromomethyl)-4-methoxy-2-nitrobenzene
https://huagongshe.com/reaction/1678709
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Methyl-3-nitroanisole | HCID 87137 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 1-(Bromomethyl)-4-methoxy-2-nitrobenzene | HCID 3747830 | — |
Reaction Steps
4-Methyl-3-nitroanisole (2.7 mL; manufactured by Sigma-Aldrich Co.) was dissolved in carbon tetrachloride (20 mL; manufactured by Wako Pure Chemical Industries, Ltd.), and NBS (4.0520 g; manufactured by Tokyo Chemical Industry Co., Ltd.) and hydrated benzoyl peroxide (348 mg; manufactured by Sigma-Aldrich Co.) were added to the solution. The mixture was purged with nitrogen, and was stirred for 3 hours at reflux. The reaction solution was filtered, and then the filtrate was washed with an aqueous solution of NaHSO3 and water and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by column chromatography (“COLUMN-B”; n-hexane:ethyl acetate=94:6→73:27). Thus, the title compound (3.2549 g) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08008506B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-160003e9764547afa9c7eb3bf7cabab0 |
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| Source note | uspto-grants-2011_08 |
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