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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418196Generated: November 1, 2026

Azobisisobutyronitrile → Methyl 4-(bromomethyl)-2-methoxybenzoate

https://huagongshe.com/reaction/1418196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantSodium SulfiteHCID 24437—
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 2-methoxy-4-methylbenzoateHCID 7172021—
SolventCarbon TetrachlorideHCID 5943—
ProductMethyl 4-(bromomethyl)-2-methoxybenzoateHCID 11288398—

Reaction Conditions

Temperature70 °C

Reaction Steps

9.07 g (51.0 mmol) of N-bromosuccinimide and 120 mg of azobis(isobutyronitrile) were added to a solution of 7.64 g (42.4 mmol) of methyl 4-methyl-2-methoxybenzoate in 140 ml of carbon tetrachloride under a stream of nitrogen, and the resulting mixture was stirred at 70° C. for 1 hour. A further 200 mg of azobis(isobutyronitrile) were then added, making a total addition of 320 mg (1.95 mmol). The reaction mixture was then stirred for 1 hour, after which an aqueous solution of sodium sulfite was added to the mixture to decompose any excess of the reagent. The organic phase was concentrated by evaporation under reduced pressure to one-fourth of its original volume. The concentrate was diluted with ethyl acetate, and the diluted solution was washed with a saturated aqueous solution of sodium hydrogencarbonate, with water and with a saturated aqueous solution of sodium chloride, in that order, after which it was dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure, giving 11.26 of crude methyl 4-bromomethyl-2-methoxybenzoate as a residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05880147
Source datasetuspto-grants-1999_03
ORD IDord-09d725cea6554e60947d67272c95a7b4
Source noteuspto-grants-1999_03