Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091863Generated: November 1, 2026

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

https://huagongshe.com/reaction/1091863

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 numberUS08129401B2
Source datasetuspto-grants-2012_03
ORD IDord-d7a617cdb1dc4b7bb00aeee2f2b41e37
Source noteuspto-grants-2012_03