HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-(1H-Indol-5-ylmethyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | (1H-indol-5-yl)methanamine | HCID 54791 | — |
| Product | N-(1H-Indol-5-ylmethyl)acetamide | HCID 22139217 | 96% |
Reaction Steps
The synthesis was performed with reference to the known literature (International Patent Publication WO2000/75139). 5-Aminomethyl-1H-indole (0.50 g, 3.4 mmol) was added with acetic anhydride (2.0 mL), and the mixture was stirred at room temperature for 3 hours. The mixture was azeotroped twice with toluene under reduced pressure, and the residual solid was washed with ethyl acetate to obtain N-[(1H-indol-5-yl)methyl]acetamide (0.62 g, 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09156827B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-fb0ba0cfb4bc4b87be96f1f84ff06edb |
| Source note | uspto-grants-2015_10 |