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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460280Generated: October 29, 2026

Pyridiniumtribromide → 7-Bromo-5-isobutyl-3,3-dimethyl-2,3-dihydro-benzofuran

https://huagongshe.com/reaction/460280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridiniumtribromideHCID 21124087—
Reactant5-Isobutyl-3,3-dimethyl-2,3-dihydro-benzofuranHCID 22041397—
SolventDichloromethaneHCID 6344—
Product7-Bromo-5-isobutyl-3,3-dimethyl-2,3-dihydro-benzofuranHCID 2204141068.5%

Reaction Steps

To a solution of 5-isobutyl-3,3-dimethyl-2,3-dihydro-benzofuran (1.59 g, 7.78 mmol) in dichloromethane (40 mL) was added pyridinium tribromide (2.49 g, 7.78 mmol) and the reaction mixture stirred at room temperature overnight. The solution was washed with water and brine, dried (MgSO4), filtered and evaporated. The residue was purified on silica gel (0% to 2% ethyl acetate in hexane) to give 1.51 g of 7-bromo-5-isobutyl-3,3-dimethyl-2,3-dihydro-benzofuran (68%). 1H NMR (300 MHz; CDCl3): δ 0.90 (d, J=6.3 Hz, 6H), 1.33 (s, 6H), 1.77 (m, 1H), 2.39 (d, J=7.5 Hz, 2H), 4.30 (s, 2H), 6.80 (d, J=1.5 Hz, 1H), 7.05 (d, J=1.5 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196108B2
Source datasetuspto-grants-2007_03
ORD IDord-3ebd96619f584988882e4ef33576ddad
Source noteuspto-grants-2007_03