HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 4-nitrophenylacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | (4-Nitrophenyl)acetic acid | HCID 4661 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Product | Ethyl 4-nitrophenylacetate | HCID 79517 | 98% |
Reaction Steps
To a stirred solution of (4-nitro-phenyl)-acetic acid (3 g, 16.4 mmol) in ethanol (30 mL) was added sulphuric acid (1 mL) and the reaction mixture was heated to reflux for 16 hours. The reaction mixture was neutralized with 2N aq. NaOH solution and extracted with EtOAc (3×50 mL). The combined organic layers were dried (Na2SO4) and evaporated in vacuo to afford the title compound as a light yellow oil in 98% yield, 3.4 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846698B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-6b9f9ab498404a8ab71a0ea8bcffc870 |
| Source note | uspto-grants-2014_09 |