HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 11013758, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 11023487 | HCID 11023487 | — |
| Product | HCID 11013758 | HCID 11013758 | 88% |
Reaction Steps
0.72 g (2.2 mmoles) of 7-chloro-4-methyl-1-(4-nitrophenyl)-4,5-dihydro-3H-2,3-benzodiazepine are stirred in 4 ml of acetic anhydride at 25° C. for 3 hours, then the reaction mixture is poured onto 20 ml of ice water, the crystalline product is filtered and washed with water several times. The crude product obtained is purified by suspending it in 4 ml of hot ethanol. After filtration and drying, 0.69 g (88%) of the title compound are obtained M.p.: 174°-175° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05807851 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-acea4f7cfb8145d7b02f73b53fb3f6f7 |
| Source note | uspto-grants-1998_09 |