HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 4-Bromo-7-methoxy-2-methoxymethylbenzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 7-Methoxy-2-methoxymethylbenzofuran | HCID 18423640 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Bromo-7-methoxy-2-methoxymethylbenzofuran | HCID 18423639 | 110.7% |
Reaction Steps
A solution of 7-methoxy-2-methoxymethylbenzofuran (13.32 g) in acetonitrile (500 ml) was stirred at room temperature. N-bromosuccinimide (11.04 g) was added and stirring continued for 2 days after which the solvent was removed in vacuo. The resulting oil was partitioned between ethyl acetate (100 ml) and sodium metasulfite solution (50 ml), the organic extract washed with more sodium metasulfite solution (2×50 ml), followed by brine (50 ml). The organic layer was separated, dried over magnesium sulphate, filtered and the solvent removed in vacuo to afford the title compound as a yellow oil (18.61 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06331556B2 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-539731bc6a884ee399288dab12ae68e7 |
| Source note | uspto-grants-2001_12 |