HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrobenzyl chloride → 4-[(2-isopropyl-1H-benzimidazol-1-yl)methyl]aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrobenzyl chloride | HCID 7482 | — |
| Reactant | 2-(propan-2-yl)-1H-1,3-benzodiazole | HCID 22121 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-[(2-isopropyl-1H-benzimidazol-1-yl)methyl]aniline | HCID 22392788 | — |
Reaction Steps
A solution of 2-isopropylbenzimidazole (4.0 g, 25 mmol) in THF was treated with sodium hydride (1.00 g, 25 mmol, 60% dispersed in oil) under N2 atmosphere and stirred for 2 hr. 4-Chloromethyl-1-nitrobenzene (4.3 g, 25 mmol) was added and the reaction stirred for 16 hr. The reaction was worked by extraction from NaHCO3 with EtOAc×3, the combined organic layers were dried with MgSO4, filtered, and concentrated. This material was converted to the aniline as shown in Example 200. MS found: (M+H)=267.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06890915B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-603c814a0c3f457bb1113056384d0dd0 |
| Source note | uspto-grants-2005_05 |