HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 66704013, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 66704006 | HCID 66704006 | — |
| Product | HCID 66704013 | HCID 66704013 | — |
Reaction Steps
600 mg of 6-chloro-2-ethylamino 4-(4-nitrophenyl)quinoline (compound 2a) were added to 0.19 g of acetic anhydride. The mixture was boiled at 70° C. for 4 hours and cooled, and the acetic anhydride was removed by distillation. The residue was mixed with water, extracted with ethyl acetate and washed with water, and the product was obtained as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08106204B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-f6cbee7c1f734408bc48ac35add165fa |
| Source note | uspto-grants-2012_01 |