HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → methyl (2Z)-2-bromo-2-[(2-chlorophenyl)hydrazinylidene]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | methyl (2E)-2-[(2-chlorophenyl)hydrazinylidene]acetate | HCID 19868318 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | methyl (2Z)-2-bromo-2-[(2-chlorophenyl)hydrazinylidene]acetate | HCID 140475537 | 71.3% |
Reaction Steps
To a solution of the title compound of Step A (16.5 g, 77 mmol) in tetrahydrofuran (150 mL) was added N-bromosuccinimide (13.7 g, 77 mmol) and the mixture was stirred at ambient temperature for 2 hours. The mixture was concentrated and extracted with hexane and the hexane solution was concentrated to give the title compound of Step B (16 g) as an orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07087598B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-a30fcfbaca0f4f4f879d97038b13ac03 |
| Source note | uspto-grants-2006_08 |