Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14476Generated: October 30, 2026

N-bromobutanimide → 7-Amino-8-bromo-3-(4-chlorophenyl)-2-isopropyl-chromen-4-one

https://huagongshe.com/reaction/14476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant7-Amino-3-(4-chlorophenyl)-2-isopropyl-chromen-4-oneHCID 11681190—
SolventChloroformHCID 6212—
Product7-Amino-8-bromo-3-(4-chlorophenyl)-2-isopropyl-chromen-4-oneHCID 59724244—

Reaction Steps

A stirred solution of 7-amino-3-(4-chlorophenyl)-2-isopropyl-chromen-4-one (0.36 g, 1.15 mmol) in chloroform (10 ml) is treated at room temperature with N-bromosuccinimide (0.21 g, 1.2 mmol, 1.05 eq.). After stirring for 20 min, the mixture is partitioned between water (150 ml) and ethyl acetate (50 ml). The organic phase is washed with brine (100 ml), dried (magnesium sulfate) and filtered, and the solvent is removed by evaporation in vacuo to afford the title compound as an orange solid. The product is used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732435B2
Source datasetuspto-grants-2010_06
ORD IDord-28bc31faf3b746c18256815d2d2dd775
Source noteuspto-grants-2010_06