HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 4-bromo-2,2-dimethyl-5-(thiazol-4-yl)furan-3(2H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2,2-dimethyl-5-(thiazol-4-yl)furan-3(2H)-one | HCID 59354805 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-bromo-2,2-dimethyl-5-(thiazol-4-yl)furan-3(2H)-one | HCID 59354852 | 71% |
Reaction Steps
To a stirred solution of 2,2-dimethyl-5-(thiazol-4-yl)furan-3(2H)-one (90 mg, 0.46 mmol) in CHCl3 (1.8 mL) was added NBS (0.12 g, 0.69 mmol) portionwise at RT and the reaction mixture was stirred for 1 h. The reaction mixture was diluted with DCM (10 mL), washed with water (5 mL), brine (10 mL), dried over Na2SO4, filtered and then concentrated in vacuo to obtain the crude product. The crude material was purified via silica gel column chromatography to afford 4-bromo-2,2-dimethyl-5-(thiazol-4-yl)furan-3(2H)-one (40 mg, 71%) as an off white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08071595B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-cbad0e207f2c4965a376ecb02b7199f0 |
| Source note | uspto-grants-2011_12 |