Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188012Generated: October 29, 2026

N-bromobutanimide → Ethyl 2-bromomethyl-6-methoxybenzoate

https://huagongshe.com/reaction/2188012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Methoxy-6-methyl-benzoic acid ethyl esterHCID 591060—
CatalystAzobisisobutyronitrileHCID 6547—
SolventCarbon TetrachlorideHCID 5943—
ProductEthyl 2-bromomethyl-6-methoxybenzoateHCID 1003892685%

Reaction Steps

2-Methoxy-6-methylbenzoic acid ethyl ester (500 mg, 2.67 mmol), N-bromosuccinimide (483.8 mg, 2.72 mmol) and 2,2′-azobis(2-methyl-propionitrile) (30.2 mg, 0.123 mmol) in carbon tetrachloride (10 ml) were heated to reflux. After 18 hours, the reaction mixture was evaporated to dryness in vacuo. The residue was dissolved in dichloromethane (100 ml) and washed with water (2×50 ml). The organic layer was dried (MgSO4), filtered and the solvent evaporated in vacuo. The residue (702 mg) was purified by column chromatography using a mixture of hexanes/dichloromethane (1:1) as eluent, which afforded 573 mg (85%) of 6-bromomethyl-2-methoxy-benzoic acid ethyl ester as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410556B1
Source datasetuspto-grants-2002_06
ORD IDord-cc465524f3c54e1ab1319e52cd5fbc82
Source noteuspto-grants-2002_06