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 Bicarbonate | HCID 516892 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-(2,3-Dihydro-1H-inden-2-yl)acetamide | HCID 12452137 | 49,435.398% |
Reaction Steps
A mixture of 2-aminoindan hydrochloride (13.3 g, 78 mmol), acetic anhydride (6 g, 0.157 mmol) and saturated sodium bicarbonate (100 mL) in ether (100 mL) was stirred at room temperature for 1 h. The organic phase was separated, and the aqueous layer back washed with ether. The combined organic layer was washed with saturated chloride solution, dried over magnesium sulfate, filtered and evaporated to give the acetamide (13.6 g) in quantitative yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05721234 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-c8f79b0d59fa4908974658cecc34cd43 |
| Source note | uspto-grants-1998_02 |