HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 1-Acetyl-6-(methylthio)-benz[cd]indol-2-(1H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 6-(Methylthio)benz[cd]indol-2(1H)-one | HCID 19750824 | — |
| Product | 1-Acetyl-6-(methylthio)-benz[cd]indol-2-(1H)-one | HCID 19750828 | — |
Reaction Steps
A mixture of 1 g of 6-(methylthio)-benz[cd]-indol-2(1H)-one (Example 2) and 10 ml of acetic anhydride is stirred and heated at reflux for 2 hours, cooled and filtered. The cake is washed with ethanol and ether then dried. The dried cake is suspended in 15 ml of hot ethanol, filtered and the cake crystallized from 150 ml of ethanol to afford the desired product as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05229411 |
| Source dataset | uspto-grants-1993_07 |
| ORD ID | ord-baf31a8f9aaf4b7d937c1479ff9364c5 |
| Source note | uspto-grants-1993_07 |