HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64863Generated: October 27, 2026
Hydrochloric Acid → 5-Dimethylamino-2-nitrobenzylamine
https://huagongshe.com/reaction/64863
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-(Dimethylamino)-2-nitrobenzonitrile | HCID 20235840 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Dimethylamino-2-nitrobenzylamine | HCID 20235839 | — |
Reaction Steps
A solution consisting of 120 ml of trifluoroacetic acid and 200 ml of tetrahydrofuran was added to a solution of 60 g of sodium borohydride in 300 ml of tetrahydrofuran under ice-cooling to a temperature of 15° C. or less. 63.4 of 5-dimethylamino-2-nitrobenzonitrile was added to the mixture, followed by stirring. After cooling the heat generated, the stirring was continued at room temperature overnight. 650 ml of a 10% aqueous solution of hydrochloric acid was then added thereto, followed by heat-refluxing for 1.5 hours. The tetrahydrofuran was removed by distillation under reduced pressure. The aqueous layer was washed with benzene, rendered alkaline with a sodium hydroxide aqueous solution, and extracted with chloroform. The extract was washed with water, dried and distilled off to remove the chloroform. The residue was purified by silica gel chromatography to obtain 33.4 g of 5-dimethylamino-2-nitrobenzylamine (melting point: 97°-98° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04610987 |
|---|
| Source dataset | uspto-grants-1986_09 |
|---|
| ORD ID | ord-37edea4d20d6431ba47637f5b7c59747 |
|---|
| Source note | uspto-grants-1986_09 |
|---|