HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-(3,4-Dichlorobenzyl)-5-acetoxyindole-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | N-(3,4-Dichlorobenzyl)-5-hydroxyindole-2-carboxylic acid | HCID 9949615 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(3,4-Dichlorobenzyl)-5-acetoxyindole-2-carboxylic acid | HCID 22718737 | — |
Reaction Steps
To a solution of N-(3,4-Dichlorobenzyl)-5-hydroxyindole-2-carboxylic acid (10 g) in warm ethyl acetate (250 ml) was added 4-dimethylaminopyridine (100 mg) and acetic anhydride (5.0 ml) and the resulting mixture was stirred for 2 hours. The organics were washed with 1N HCl and dried. Hexane was added to cause crystallision of the product. The solid was filtered and washed with hexane to give the desired product. (5 g, 44%). 1H NMR (DMSO-d6) δ 2.25 (s, 3H), 5.85 (s, 2H), 6.9 (dd, 1H), 7.05 (dd, 1H), 7.3-7.6 (m, 5H); m/z 378, 380 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06737435B1 |
| Source dataset | uspto-grants-2004_05 |
| ORD ID | ord-8f74b749bf5d4e83a3d8fe9045f41b9c |
| Source note | uspto-grants-2004_05 |