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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2270119Generated: October 31, 2026

N-bromobutanimide → 4-Bromo-7-methoxy-2-methoxymethylbenzofuran

https://huagongshe.com/reaction/2270119

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant7-Methoxy-2-methoxymethylbenzofuranHCID 18423640—
SolventAcetonitrileHCID 6342—
Product4-Bromo-7-methoxy-2-methoxymethylbenzofuranHCID 18423639110.7%

Reaction Steps

A solution of 7-methoxy-2-methoxymethylbenzofuran (13.32 g) in acetonitrile (500 ml) was stirred at room temperature. N-bromosuccinimide (11.04 g) was added and stirring continued for 2 days after which the solvent was removed in vacuo. The resulting oil was partitioned between ethyl acetate (100 ml) and sodium metasulfite solution (50 ml), the organic extract washed with more sodium metasulfite solution (2×50 ml), followed by brine (50 ml). The organic layer was separated, dried over magnesium sulphate, filtered and the solvent removed in vacuo to afford the title compound as a yellow oil (18.61 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06331556B2
Source datasetuspto-grants-2001_12
ORD IDord-539731bc6a884ee399288dab12ae68e7
Source noteuspto-grants-2001_12