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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548970Generated: November 1, 2026

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

https://huagongshe.com/reaction/548970

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 numberUS07943634B2
Source datasetuspto-grants-2011_05
ORD IDord-9ee6404e85414c068db05b0ecc9a32a9
Source noteuspto-grants-2011_05