HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 2-Acetamido-5-(4-nitrobenzyl)-4-propylthiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-Amino-5-(4-nitrobenzyl)-4-propylthiazole | HCID 19775545 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Product | 2-Acetamido-5-(4-nitrobenzyl)-4-propylthiazole | HCID 19775558 | — |
Reaction Steps
2 g (7.2 mmol) of 2-amino-5-(4-nitrobenzyl)-4-propylthiazole in 2.5 ml of acetic anhydride, in the presence of 88 mg of 4-dimethylaminopyridine (0.72 mmol), are heated at 80° C. for 1 hour. As the reaction mixture is cooled, the formation of a precipitate is observed. This is filtered off and washed with ether to give 1.6 g of the derivative 2-acetamido-5-(4-nitrobenzyl)-4-propylthiazole, which is pale yellow solid melting at 170° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05192781 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-99b661cd7b664243a7b59ff01b96cc47 |
| Source note | uspto-grants-1993_03 |