Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1407521Generated: October 30, 2026

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

https://huagongshe.com/reaction/1407521

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 numberUS08916580B2
Source datasetuspto-grants-2014_12
ORD IDord-2b963be2827845c39bb55a6429131886
Source noteuspto-grants-2014_12