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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1965371Generated: November 1, 2026

N-bromobutanimide → 7-Bromo-5-fluoro-2,3-dihydro-1,4-benzodioxine

https://huagongshe.com/reaction/1965371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant5-Fluoro-2,3-dihydro-1,4-benzodioxineHCID 12464522—
SolventMethanolHCID 887—
Product7-Bromo-5-fluoro-2,3-dihydro-1,4-benzodioxineHCID 6860117787.5%

Reaction Steps

A solution of 5-fluoro-2,3-dihydrobenzo[b][1,4]dioxine (1.54 g, 10.0 mmol) and 1-bromopyrrolidine-2,5-dione (1.8 g, 10 mmol) in methanol (20 mL) was heated at reflux for 0.5 h, allowed to cool to ambient temperature and concentrated in vacuo. The residue was taken up in dichloromethane (50 mL) and washed with water (50 mL). The organic phase was dried over magnesium sulfate, filtered and concentrated in vacuo. Purification of the residue by column chromatography eluted with a 0% to 30% gradient of ethyl acetate in hexanes afforded 7-bromo-5-fluoro-2,3-dihydrobenzo[b][1,4]dioxine (2.04 g, 87%) as a colorless solid: MS (ES+) m/z 233.6 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415370B2
Source datasetuspto-grants-2013_04
ORD IDord-3e10c0ba6a494923a8a9e16ffe3855c6
Source noteuspto-grants-2013_04