HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 22145880, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 22145850 | HCID 22145850 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22145880 | HCID 22145880 | — |
Reaction Steps
Acetic anhydride (10 mL) is treated with N-(2,6-dichloro-4-aminophenyl)-3-cyclopentyloxy-4-methoxybenzamide (0.8 g), and the reaction mixture is stirred for 2 hours and left to stand overnight. It is then poured into water (100 mL), and extracted with ethyl acetate (100 mL) and then with dichloromethane (100 mL). The organic extracts are combined, dried over magnesium sulfate, and evaporated, to give N-(4-acetylamino-2,6-dichlorophenyl)-3-cyclopentyloxy-4-methoxybenzamide (0.4 g), m.p. 250-252° C. [Elemental analysis: C, 57.6; H, 5.05; N, 6.3; Cl, 16.1%; calculated: C, 57.5; H, 5.1; N, 6.4; Cl, 16.2%].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06472412B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-c521521b84eb4fd1b5282ad01f95f2b4 |
| Source note | uspto-grants-2002_10 |