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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906814Generated: October 31, 2026

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

https://huagongshe.com/reaction/906814

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 numberUS08012997B2
Source datasetuspto-grants-2011_09
ORD IDord-1517f3113a9e47e1bedeb190e1609fe0
Source noteuspto-grants-2011_09