Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272217Generated: November 2, 2026

N-bromobutanimide → 1345120-02-6

https://huagongshe.com/reaction/2272217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Bromo-5-chlorophenolHCID 13284272—
Reactant6-Chloro-2,3-dihydro-1-benzofuranHCID 15467087—
ReactantHCID 67126933HCID 67126933—
SolventAcetonitrileHCID 6342—
Product1345120-02-6HCID 58487295—

Reaction Steps

In a similar way as described above, 6-chloro-2,3-dihydrobenzofuran (142) was prepared starting from 2-bromo-5-chlorophenol. NBS (155 mg, 0.87 mmol) was added to a solution of 2-bromo-5-chloro-2,3-dihydrobenzo[b]furan (142) (135 mg, 0.87 mmol) in 5 ml ACN. The reaction mixture was stirred 5 h at r.t. The yellow solution was poured into ice-water, extracted with EA. Org. phase was washed with aq. sodium bicarbonate and brine subsequently. After dried over sodium sulfate the org. phase was concentrated to give 204 mg (purity>90%, quantitative yield) title compound as pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120751B2
Source datasetuspto-grants-2015_09
ORD IDord-03d46d173c4c439ca4c2d9d7c559bf93
Source noteuspto-grants-2015_09