HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 7-Amino-8-bromo-3-(4-chlorophenyl)-2-isopropyl-chromen-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 7-Amino-3-(4-chlorophenyl)-2-isopropyl-chromen-4-one | HCID 11681190 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 7-Amino-8-bromo-3-(4-chlorophenyl)-2-isopropyl-chromen-4-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07732435B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-28bc31faf3b746c18256815d2d2dd775 |
| Source note | uspto-grants-2010_06 |