Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Boron trifluoride | HCID 6356 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | N-(2-aminophenyl)-3,5-di-t-butyl-4-hydroxybenzamide | HCID 23370116 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23370072 | HCID 23370072 | 68.2% |
Reaction Steps
To a suspension of sodium borohydride (2.72 g) in tetrahydrofuran (80 ml) was added dropwise under ice-cooling BF3, Et20 (8.86 ml) and the mixture was stirred for 30 minutes. To this mixture was added by portions N-(2-aminophenyl )-3,5-di-t-butyl-4-hydroxybenzamide (3.06 g ) and the mixture was stirred overnight while returning slowly to room temperature. 6N hydrochloric acid war added and the mixture was heated under reflux for 30 minutes, the solvent was distilled off and the residue was placed into water, neutralized with sodium hydrogen carbonate, extracted with ethyl acetate, washed with water and saturated saline and dried over anhydrous MgSO4. The solvent was distilled off and the residue was purified by a silica gel column chromatography (hexane:ethyl acetate=4:1) to give (2-aminophenyl)-3,5-di-t-butyl-4-hydroxybenzylamine (2.00 g, 68%) as crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05576335 |
|---|
| Source dataset | uspto-grants-1996_11 |
|---|
| ORD ID | ord-5bf23823dd06442684d777b9a9816bfa |
|---|
| Source note | uspto-grants-1996_11 |
|---|