HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 5-(Benzyloxy)-4-methoxy-2-nitrobenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Benzyl 5-(benzyloxy)-4-methoxy-2-nitrobenzoate | HCID 59362000 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(Benzyloxy)-4-methoxy-2-nitrobenzoic acid | HCID 821220 | 94.7% |
Reaction Steps
To a solution of benzyl 5-(benzyloxy)-4-methoxy-2-nitrobenzoate (1.4 g, 3.56 mmol) in EtOH (10 mL) was added 1N NaOH (4.27 mL, 4.27 mmol). The mixture was stirred at RT for 1 h, upon which an additional aliquot of NaOH (4.27 mL, 4.27 mmol) was added. Stirring was continued at RT overnight. The mixture was diluted with water (20 mL) and washed with CH2Cl2 (2×25 mL). The aqueous layer was acidified to pH=2 with 0.5 N HCl and extracted with EtOAc (3×50 mL). The combined organics were dried (Na2SO4), filtered and concentrated in vacuo to give 5-(benzyloxy)-4-methoxy-2-nitrobenzoic acid (1.02 g, 3.37 mmol, 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08916576B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-671cba4a46f94d59b31cfe80a7a31a1c |
| Source note | uspto-grants-2014_12 |