HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 53640973, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 20477712 | HCID 20477712 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 53640973 | HCID 53640973 | 30% |
Reaction Steps
To a stirred solution of 1.6 g. (5 mM) of 1-(thiazolin-2-yl)-2-amino-6-(α-methylenebenzyl)benzimidazole in 150 ml. of tetrahydrofuran were added in one portion 900 mg. (0.5 mM) of N-bromosuccinimide. The reaction mixture was stirred at room temperature for seventy-two hours, and then was concentrated to a volume of about 10 ml. by evaporation of the solvent under reduced pressure. The reaction mixture was diluted with 20 ml. of water, and the crystalline precipitate that formed was collected by filtration and identified as 600 mg. of 1-(thiazolin-2-yl)-2-amino-6-(α-bromomethylenebenzyl)benzimidazole. M.P. 197°-199° C. Yield 30%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04420479 |
| Source dataset | uspto-grants-1983_12 |
| ORD ID | ord-12c91b8260ff46f1b0dc9265a0044ddc |
| Source note | uspto-grants-1983_12 |