HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 4-bromo-2,2-dimethyl-5-(4-nitrophenyl)furan-3(2H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2,2-dimethyl-5-(4-nitrophenyl)furan-3(2H)-one | HCID 59354770 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-bromo-2,2-dimethyl-5-(4-nitrophenyl)furan-3(2H)-one | HCID 59354757 | 44% |
Reaction Steps
To a 0° C. stirred solution of crude 2,2-dimethyl-5-(4-nitrophenyl)furan-3(2H)-one (170 mg, 0.73 mmol, 1 eq) in CHCl3 (10 mL) was added NBS (259 mg, 1.45 mmol, 2 eq), and the reaction mixture was then stirred at RT for 2 h. The chloroform was removed and the crude material was then purified via silica gel column chromatography eluting with 10% EtOAc in hexanes to afford 4-bromo-2,2-dimethyl-5-(4-nitrophenyl)furan-3(2H)-one (100 mg, 44%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08071595B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-b0f9644750e14f6691938545cefd646e |
| Source note | uspto-grants-2011_12 |