HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → O-Ethylacetanilide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | N-Ethylaniline | HCID 7670 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Product | O-Ethylacetanilide | HCID 36332 | — |
Reaction Steps
To the stirred solution of commercially available ethyl aniline (20.3 g, 167.5 mmol, 1 eq.) in anhydrous pyridine (90 mL), 0° C., under argon was added acetic anhydride (32 mL, 335.04 mmol, 2 eq). After the addition, the resulting solution was stirred with warming to room temperature overnight. The reaction solution was cooled (zero degree), pH adjusted between 4 to 5 with 10% HCl, and extracted with ethyl acetate (2×500 mL). The combined organics were washed with brine, dried (Na2SO4), filtered and concentrated to provide the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08785434B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-287ccd93801b4c16a677f4601c607ab8 |
| Source note | uspto-grants-2014_07 |