HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → tert-butyl 2-(bromomethyl)-1H-benzo[d]imidazole-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | tert-butyl2-methyl-1H-benzo[d]imidazole-1-carboxylate | HCID 11183867 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | tert-butyl 2-(bromomethyl)-1H-benzo[d]imidazole-1-carboxylate | HCID 11381356 | — |
Reaction Steps
NBS (8.43 g, 47.4 mmole) and AIBN (2.1 g, 12.8 mmole) were added to a solution of 1-BOC-2-methylbenzimidazole (10.0 g, 43.1 mmole) in CCl4 (120 mL) at reflux. After 21 hr, the reaction was cooled and filtered. The filtrate was concentrated, and the resulting brown oil was chromatographed on silica gel (15% EtOAc/hexanes) to afford the title product: 1H NMR (400 MHz, CDCl3) δ 7.94-8.01 (m, 1 H), 7.70-7.75 (m, 1 H), 7.31-7.44 (m, 2 H), 4.96 (s, 2 H), 1.75 (s, 9 H),
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05977101 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-286272d812cf4264924507aed5b12056 |
| Source note | uspto-grants-1999_11 |