HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-(2,3-Dihydro-1H-inden-2-yl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-Aminoindan hydrochloride | HCID 122764 | — |
| Reactant | Sodium Acetate Trihydrate | HCID 23665404 | — |
| Product | N-(2,3-Dihydro-1H-inden-2-yl)acetamide | HCID 12452137 | — |
Reaction Steps
25 g. of 2-indanamine hydrochloride (0.15 mole), 20 g. of sodium acetate trihydrate (0.14 mole), and 40 g. of acetic anhydride (0.4 mole) were stirred at 25° C. for sixteen hours. The mixture was evaporated and the residue was partitioned between chloroform and water. The chloroform extracts were pooled, washed with 10% hydrochloric acid and then with 5% aqueous sodium carbonate, dried and evaporated to yield N-acetyl-2-indanamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04192888 |
| Source dataset | uspto-grants-1980_03 |
| ORD ID | ord-d86580684e1241d2bd4b0cb4777a8409 |
| Source note | uspto-grants-1980_03 |