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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369932Generated: October 31, 2026

Benzoyl Peroxide → Methyl 3-(bromomethyl)-2-fluorobenzoate

https://huagongshe.com/reaction/2369932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 2-fluoro-3-methylbenzoateHCID 22049929—
SolventCarbon TetrachlorideHCID 5943—
ProductMethyl 3-(bromomethyl)-2-fluorobenzoateHCID 2205004456.6%

Reaction Steps

To a solution of methyl 2-fluoro-3-methylbenzoate (13.8 g, 82.3 mmol) from Step A above and N-bromosuccinimide (16.0 g, 90.6 mmol) in carbon tetrachloride (82 mL) at room temperature was added a catalytic amount of benzoyl peroxide. The yellow mixture was heated under reflux until the reaction was complete by TLC (overnight) and then it was concentrated and purified by column chromatography (silica gel, 9:1 hexanes/ethyl acetate) to afford methyl 3-(bromomethyl)-2-fluorobenzoate as a light yellow oil (11.5 g, 56%): 1H NMR (500 MHz, CDCl3) δ 7.90 (t, J=8.0 Hz, 1H), 7.59 (t, J=7.5 Hz, 1H), 7.19 (t, J=7.5 Hz, 1H), 4.53 (s, 2H), 3.90 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710046B2
Source datasetuspto-grants-2014_04
ORD IDord-f0faca8807264bb1adc3c0e9c5330a75
Source noteuspto-grants-2014_04