HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → (3-Benzylamino-phenyl)-carbamic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | tert-butyl N-(3-aminophenyl)carbamate | HCID 12877220 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3-Benzylamino-phenyl)-carbamic acid tert-butyl ester | HCID 67229700 | — |
Reaction Steps
A solution of (3-amino-phenyl)-carbamic acid tert-butyl ester (1 g, 4.8 mmol), benzaldehyde (0.54 ml, 5.3 mmol) and acetic acid (0.41 ml, 7.2 mmol) in dry tetrahydrofuran (30 ml) were stirred at room temperature for 2 hrs. Sodium borohydride (0.172 g, 4.5 mmol) was added and the reaction stirred at room temperature overnight. The reaction mixture was quenched with water (50 ml) and extracted with dichloromethane (3×50 ml). The combined organics were dried (magnesium sulphate), concentrated in vacuo and the crude residue purified by flash column chromatography (SiO2) eluting with ethyl acetate to afford the title compound as an off white solid (1.27 g, 89%) HPLC retention time 6.4 min. Mass spectrum (ES+) m/z 198 (M+H-BOC)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08372840B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-6d428428c64741a0a9545bbc31f9dadf |
| Source note | uspto-grants-2013_02 |