HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 23458908, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Benzoic acid, 4-[[(4-chlorophenyl)methyl]amino]-, ethyl ester | HCID 773384 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 23458908 | HCID 23458908 | 63% |
Reaction Steps
Ethyl 4-(4-chlorobenzylamino)-benzoate (11.56 g; 0.04 M), acetic anhydride (40 ml) and concentrated sulphuric acid (5 drops) were mixed and heated with stirring on a steam-bath for 1 hour. The mixture was cooled to room temperature, added to iced water (100 ml) and neutralised with solid sodium bicarbonate. The product was extracted into dichloromethane (2×100 ml), washed with water (1×100 ml) and evaporated to give an oil from which N-(4-ethoxycarbonylphenyl)-N-(4-chlorobenzyl)-acetamide (8.32 g; 63%) was obtained by chromatography on silica-gel in dichloromethane then 2% methanol-dichloromethane followed by crystallisation from ethanol. M.p. 65°-6° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04271188 |
| Source dataset | uspto-grants-1981_06 |
| ORD ID | ord-7aa6d29ddb1740e9a9087249cee9ec62 |
| Source note | uspto-grants-1981_06 |