HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 20529234, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 20529239 | HCID 20529239 | — |
| Product | HCID 20529234 | HCID 20529234 | — |
Reaction Steps
A mixture of 10.0 g (0.05 mol) of 2,3,4,9-tetrahydro-N-methyl-1H-carbazol-2-amine and 70 ml of acetic anhydride was heated at reflux until complete solution occurred (2-3 min). After standing overnight at room temperature and further cooling at 0°, the precipitated solid was filtered, washed first with small portions of cold acetic anhydride and then thoroughly with anhydrous ether. The crude product was recrystallized from ethanol to give the title compound, mp 215°-216°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04343812 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-f260fdb95519483a82452841833e0e24 |
| Source note | uspto-grants-1982_08 |