HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 59354846, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 59354861 | HCID 59354861 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 59354846 | HCID 59354846 | 107.2% |
Reaction Steps
To a room temperature solution of 5-(4-(benzyloxy)phenyl)-2,2-dimethylfuran-3(2H)-one (1.5 g, 0.005 mol) in CHCl3 (50 mL), NBS (1.37 g, 0.007 mol) was added portionwise. The reaction mixture was stirred for 2 h at RT and then concentrated in vacuo to obtain the crude product. The residue was partitioned between water and DCM. The organic layer was separated, washed with water, dried over Na2SO4, and concentrated in vacuo to afford 5-(4-(benzyloxy)phenyl)-4-bromo-2,2-dimethylfuran-3(2H)-one (2.0 g) as a solid. This material was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08933074B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-770d4b1afe554fe88b12770d0a5acfdb |
| Source note | uspto-grants-2015_01 |