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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548995Generated: October 28, 2026

Azobisisobutyronitrile → Methyl-7-cyclopentyloxy-2-bromomethylbenzo[b]furan-4-carboxylate

https://huagongshe.com/reaction/548995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl-7-cyclopentyloxy-2-methylbenzo[b]furan-4-carboxylateHCID 44247883—
SolventCarbon TetrachlorideHCID 5943—
ProductMethyl-7-cyclopentyloxy-2-bromomethylbenzo[b]furan-4-carboxylateHCID 665925605.8%

Reaction Steps

To a well stirred refluxing solution of AIBN (500 mg) and N-bromosuccinimide (30.5 g, 0.171 moles) in carbon tetrachloride (500 mL) was added a Methyl-7-cyclopentyloxy-2-methylbenzo[b]furan-4-carboxylate (43.0 g, 0.151 moles) 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 (50.0 g) 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-de4918fa7718476bbf6bb68083e39d28
Source noteuspto-grants-2011_05