HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066845Generated: October 30, 2026
Sodium hydride → N,N-dimethyl-4-(2-fluoro-5-bromobenzyloxy)butylamine
https://huagongshe.com/reaction/1066845
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(Dimethylamino)butan-1-ol | HCID 83350 | — |
| Reactant | 4-Bromo-2-(bromomethyl)-1-fluorobenzene | HCID 13553295 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N,N-dimethyl-4-(2-fluoro-5-bromobenzyloxy)butylamine | HCID 21196124 | — |
Reaction Steps
In a 50 ml flask, under a nitrogen atmosphere, 2-fluoro-5-bromobenzyl bromide (967 mg, 3.61 mmol) was dissolved in N,N-dimethylformamide (3.5 ml). To this solution sodium hydride (60%, 245 mg, 6.14 mmol) was added and the resulting mixture was stirred for ten minutes. To the reaction mixture 4-(N,N-dimethylamino)butanol (633 mg, 5.41 mmol) was added and the rsulting mixture was stirred for six hours. The progress of the reaction was monitored by thin layer chromatography. The reaction mixture was partitioned between 1 M potassium carbonate and methylene chloride. The aqueous fraction was back extracted with methylene chloride. The organic fractions were combined and dried over sodium sulfate. The solvents were removed in vacuo. The title intermediate was further purified by liquid chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06245761B1 |
|---|
| Source dataset | uspto-grants-2001_06 |
|---|
| ORD ID | ord-c9a56a87bd494283a19ff8cc7f4f6678 |
|---|
| Source note | uspto-grants-2001_06 |
|---|