HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657337Generated: October 27, 2026
N-bromobutanimide → 1-Bromo-3-(bromomethyl)-2-methoxybenzene
https://huagongshe.com/reaction/657337
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Bromo-6-methylanisole | HCID 12262648 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 1-Bromo-3-(bromomethyl)-2-methoxybenzene | HCID 57813498 | 98.6% |
Reaction Steps
1-Bromo-3-methyl-2-(methyloxy)benzene (30.3 g, 0.15 mol), NBS (28.2 g, 0.16 mol), and BPO (1.83 g, 7.55 mmol) were suspended in 300 mL of CCl4, and the mixture was heated to 80° C. over night. After cooling to room temperature, the solution was filtrated and the solid was washed with CCl4 (30 mL×2). The filtrate was washed with NaHSO3 (aq. 250 mL×2), Na2CO3 (aq. 100 mL×2), brine (100 mL) and dried over Na2SO4. After removing the solvent, 41.4 g of the crude product was obtained (yield: 97.9%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071588B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-4acff6b538bc4895aa01859aa888bc0d |
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| Source note | uspto-grants-2011_12 |
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