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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577594Generated: November 1, 2026

N-bromobutanimide → Methyl 2-(bromomethyl)-5-ethoxybenzoate

https://huagongshe.com/reaction/577594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 5-ethoxy-2-methylbenzoateHCID 86723821—
SolventCarbon TetrachlorideHCID 5943—
SolventDichloromethaneHCID 6344—
SolventSodium chloride; waterHCID 57417360—
ProductMethyl 2-(bromomethyl)-5-ethoxybenzoateHCID 8672382286.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of methyl 5-ethoxy-2-methylbenzoate (134b, 0.700 g, 3.61 mmol) in CCl4 (12 mL) was added BPO (18.0 mg, 0.0720 mmol) and NBS (0.706 g, 3.97 mmol) at room temperature. The resulting mixture was heated at 80° C. for 12 hours under N2 atmosphere. The mixture was diluted with CH2Cl2 (10 mL) and brine (3 mL). The organic layer was separated and washed with NaHCO3 (2 N, 10 mL), H2O (5 mL) and brine (5 mL), dried over Na2SO4 and concentrated under vacuum. The residue was purified by column chromatography (petroleum ether/EtOAc=5:1) to give methyl 2-(bromomethyl)-5-ethoxybenzoate (134c, 0.85 g, 86%) as yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040515B2
Source datasetuspto-grants-2015_05
ORD IDord-9039af9cf5a4456791bd97a9e6725b39
Source noteuspto-grants-2015_05