HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 2-Amino-alpha-(3-tert-butoxycarbonylaminomethylphenyl)-5-isobutyloxybenzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Amino-3'-tert-butoxycarbonylaminomethyl-5-isobutyloxy-benzophenone | HCID 18315365 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Amino-alpha-(3-tert-butoxycarbonylaminomethylphenyl)-5-isobutyloxybenzyl alcohol | HCID 54216676 | — |
Reaction Steps
In methanol (12 ml) was dissolved 2-amino-3′-tert-butoxycarbonylaminomethyl-5-isobutyloxy-benzophenone (0.38 g). To the solution was added, while stirring at room temperature, sodium borohydride (50 mg). The reaction mixture was concentrated, to which was added water, followed by extraction with ethyl acetate (50 ml). The organic layer was washed with water and dried over anhydrous sodium sulfate. The solvent was distilled off to leave 2-amino-α-(3-tert-butoxycarbonylaminomethylphenyl)-5-isobutyloxy-benzyl alcohol as a yellow oily product (0.36 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06352982B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-68faad7321444b02bb36d37ebf32d4d3 |
| Source note | uspto-grants-2002_03 |