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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782015Generated: October 29, 2026

N-bromobutanimide → 7-bromo-2,3-dihydro-1,4-benzodioxin-6-amine

https://huagongshe.com/reaction/1782015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant1,4-Benzodioxan-6-ylamineHCID 89148—
CatalystSulfuric AcidHCID 1118—
SolventTetrahydrofuranHCID 8028—
Product7-bromo-2,3-dihydro-1,4-benzodioxin-6-amineHCID 498322993%

Reaction Steps

A solution of 2,3-dihydro-benzo[1,4]dioxin-6-ylamine (1 g, 6.6 mmol) in tetrahydrofuran (15 ml) was cooled to −78 deg C. then treated with 1 drop of concentrated sulphuric acid followed by N-bromosuccinimide (1.2 g, 6.6 mmol). The mixture was allowed to warm to room temperature over 1 hour then evaporated. The residue was dissolved in ether, washed with water then brine, dried and evaporated to afford an oil (1.4 g, 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498326B2
Source datasetuspto-grants-2009_03
ORD IDord-5389309b1db84247bd8965dc569dee38
Source noteuspto-grants-2009_03