HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → benzyl N-(6-hydroxynaphthalen-2-yl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 6-Hydroxy-2-naphthoic acid | HCID 85557 | — |
| Reactant | 12-Deoxyphorbol 13-phenylacetate 20-acetate | HCID 3034821 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | benzyl N-(6-hydroxynaphthalen-2-yl)carbamate | HCID 67520229 | — |
Reaction Steps
6-Hydroxy-2-naphthoic acid (30 g, 160 mmol, Aldrich), dppa (48.4 g, 176 mmol, Aldrich), benzyl alcohol (51.8 g, 480 mmol, Aldrich) and Et3N (32.3 g, 320 mmol, Aldrich) were heated at reflux with toluene (500 mL, Aldrich) for 16 h. After cooling to RT, the volatile portion was removed in vacuo. The resulting brown residue was purified by silica gel column chromatography (40% EtOAc/hexane) to give crude compound, which was further purified by crystallization from 50% EtOAc/Hexane to give the title compound as an off-white solid. MS (ESI, pos. ion) m/z: 294.2 (M+1). Mass Calc'd for C18H15NO3: 293.11.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08178557B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-4acbdd224fdc4bd9a95b0f40a223000a |
| Source note | uspto-grants-2012_05 |