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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091833Generated: November 1, 2026

N-bromobutanimide → Methyl-2-bromomethyl-7-methoxybenzo[b]furan-4-carboxylate

https://huagongshe.com/reaction/1091833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl-7-methoxy-2-methylbenzo[b]furan-4-carboxylateHCID 66592954—
CatalystAzobisisobutyronitrileHCID 6547—
SolventCarbon TetrachlorideHCID 5943—
ProductMethyl-2-bromomethyl-7-methoxybenzo[b]furan-4-carboxylateHCID 6659298257.1%

Reaction Steps

To a well stirred refluxing solution of AIBN (40.0 mg, 1.0%) and N-bromo succinimide (3.4 g, 19.05 mmol) in carbon tetrachloride (60.0 mL) was added a Methyl-7-methoxy-2-methylbenzo[b]furan-4-carboxylate (from step 5) (4.0 g, 18.16 mmol) and refluxed for 2-3 hours. Reaction mixture was cooled to room temperature and filtered thorough Celite bed. The filtrate was concentrated under vacuo to give product (3.1 g) as brown oil. The product obtained was taken ahead for next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129401B2
Source datasetuspto-grants-2012_03
ORD IDord-69e76ed3c8cf40b6a3bc5056c99aae78
Source noteuspto-grants-2012_03