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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441143Generated: October 30, 2026

N-bromobutanimide → 7-Bromo-5-chloro-2,3-dihydro-1-benzofuran-4-amine

https://huagongshe.com/reaction/441143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant5-Chloro-2,3-dihydro-1-benzofuran-4-amineHCID 12669700—
SolventBenzeneHCID 241—
Product7-Bromo-5-chloro-2,3-dihydro-1-benzofuran-4-amineHCID 1529425787.9%

Reaction Steps

A solution of 9.1 parts of 5-chloro-2,3-dihydro-4-benzofuranamine [described in J. Het. Chem., 17(6) 1333 (1980)], 9.6 parts of N-bromosuccinimide and 130.5 parts of benzene was stirred for 1 hour at reflux temperature. The solvent was evaporated and the residue was dissolved in 387.4 parts of trichloromethane. The solution was washed with water (2×200 pans). The organic layer was dried, filtered and evaporated. The residue was purified by column chromatography (silica gel; C6H14 /CH2Cl2 50:50). The eluent of the desired fraction was evaporated, yielding 11.8 parts (87.9%) of 7-bromo-5-chloro-2,3-dihydro-4-benzofuranamine (interm. 8).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521314
Source datasetuspto-grants-1996_05
ORD IDord-c0d21305d7f7434f81f57e0e345c0d8d
Source noteuspto-grants-1996_05