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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103577Generated: October 30, 2026

N-bromobutanimide → Methyl 3-bromo-2-(bromomethyl)benzoate

https://huagongshe.com/reaction/2103577

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 3-Bromo-2-methylbenzoateHCID 12929135—
SolventAcetonitrileHCID 6342—
ProductMethyl 3-bromo-2-(bromomethyl)benzoateHCID 21907554107.2%

Reaction Steps

A mixture of methyl 3-bromo-2-methylbenzoate (17.0 g, 74.22 mmol) and N-bromosuccinimide (15.85 g, 89.06 mmol) in acetonitrile (200 mL) was heated under gently refluxing for 17 hours while a 200 W bulb situated 2 cm away was shining on the reaction flask. The mixture was cooled to room temperature and solvent was removed. The residue was dissolved in ethyl acetate (200 mL) and washed with water (3×80 mL), brine (80 mL) and dried (MgSO4). Solvent was removed to give methyl 3-bromo-2-bromomethylbenzoate (24.5 g, 97% by HPLC): 1H NMR (CDCl3) δ 7.90-7.86 (dd, J=1.0 and 7.9 Hz, 1H), 7.78-7.74 (dd, J=1.2 and 8.2 Hz, 1H), 7.22 (t, J=7.9 Hz, 1H), 5.12 (s, 2H), 3.95 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576104B2
Source datasetuspto-grants-2009_08
ORD IDord-a57000965ae241c29b2250f4e434e5c2
Source noteuspto-grants-2009_08