HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorosuccinimide → 6'-Bromo-5'-chlorospiro[cyclopentane-1,3'-indolin]-2'-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 6'-Bromospiro[cyclopentane-1,3'-indolin]-2'-one | HCID 12717090 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 6'-Bromo-5'-chlorospiro[cyclopentane-1,3'-indolin]-2'-one | HCID 66954083 | 75.4% |
Reaction Steps
N-Chlorosuccinimide (0.50 g, 3.75 mmol) was added to a solution of 6′-bromospiro[cyclopentane-1,3′-indolin]-2′-one (preparation 2, 0.20 g, 0.75 mmol) in chloroform (5 mL). The mixture was stirred and heated to reflux. After 6 hours, the mixture was cooled to room temperature. Saturated aqueous sodium hydrogen carbonate solution was added to the reaction and the mixture was extracted with chloroform. The organic layer was washed with brine, dried (MgSO4) and evaporated. Purification of the residue by flash chromatography (4:1 hexanes/ethyl acetate) gave the title compound (0.17 g, 75%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08772288B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-45ada024ac554c368d201ecc32af279a |
| Source note | uspto-grants-2014_07 |