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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Bromo-6-methylanisoleHCID 12262648—
SolventCarbon TetrachlorideHCID 5943—
Product1-Bromo-3-(bromomethyl)-2-methoxybenzeneHCID 5781349898.6%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071588B2
Source datasetuspto-grants-2011_12
ORD IDord-4acff6b538bc4895aa01859aa888bc0d
Source noteuspto-grants-2011_12