HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 5-Amino-6-(2-chlorobenzoyl)indan
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 6-(2-Chlorobenzoyl)-5-(2-chlorobenzoylamino)indan | HCID 19936583 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 5-Amino-6-(2-chlorobenzoyl)indan | HCID 19936570 | 94.4% |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
A mixture of 6-(2-chlorobenzoyl)-5-(2-chlorobenzoylamino)indan (16.0 g) and 70% H2SO4 (100 ml) was heated at 120° C. for 30 minutes and, then, poured in ice-water (300 ml). The solution was alkalinized with concentrated aqueous ammonia and extracted with ethyl acetate. The extract was washed with water and dried (MgSO4) and the solvent was distilled off to give 5-amino-6-(2-chlorobenzoyl)indan as yellow oil (10.0 g, 94.3%). Recrystallization from hexane gave yellow prisms, m.p. 90°-92°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05418239 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-47371527816841ddb6378dad826fb22b |
| Source note | uspto-grants-1995_05 |