HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 1345120-02-6
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Bromo-5-chlorophenol | HCID 13284272 | — |
| Reactant | 6-Chloro-2,3-dihydro-1-benzofuran | HCID 15467087 | — |
| Reactant | HCID 67126933 | HCID 67126933 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1345120-02-6 | HCID 58487295 | — |
Reaction Steps
In a similar way as described above, 6-chloro-2,3-dihydrobenzofuran (142) was prepared starting from 2-bromo-5-chlorophenol. NBS (155 mg, 0.87 mmol) was added to a solution of 2-bromo-5-chloro-2,3-dihydrobenzo[b]furan (142) (135 mg, 0.87 mmol) in 5 ml ACN. The reaction mixture was stirred 5 h at r.t. The yellow solution was poured into ice-water, extracted with EA. Org. phase was washed with aq. sodium bicarbonate and brine subsequently. After dried over sodium sulfate the org. phase was concentrated to give 204 mg (purity>90%, quantitative yield) title compound as pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08980629B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-98881ed90491401b8848577c63b3fd4b |
| Source note | uspto-grants-2015_03 |