HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitric Acid → Benzyl 5-(benzyloxy)-4-methoxy-2-nitrobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Benzyl 3-(benzyloxy)-4-methoxybenzoate | HCID 22070447 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | Benzyl 5-(benzyloxy)-4-methoxy-2-nitrobenzoate | HCID 59362000 | 93% |
Reaction Steps
To a solution of benzyl 3-(benzyloxy)-4-methoxybenzoate (6.32 g, 18.1 mmol) in Ac2O (62 mL) cooled to −10° C. under an atmosphere of N2 was added fuming HNO3 (1.5 mL, 37.1 mmol) in one portion. Stirring was continued at −10° C. for 10 minutes, then at RT for 3 hours. The reaction mixture was carefully poured into ice-water and the pH adjusted to ca. pH=5 with 5N NaOH, sat. NaHCO3 and 0.5 NaOH. The mixture was extracted with CH2Cl2 (3×200 mL). The combined organics were dried (Na2SO4), filtered and concentrated in vacuo. The residue was azeotroped with heptane to give benzyl 5-(benzyloxy)-4-methoxy-2-nitrobenzoate as red colored oil (6.55 g, 16.7 mmol, 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08357693B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-ebec98ad6694422eb5de10408c0727bf |
| Source note | uspto-grants-2013_01 |