HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 178487956, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | HCID 67332927 | HCID 67332927 | — |
| Product | HCID 178487956 | HCID 178487956 | — |
Reaction Steps
The title compound is prepared in analogy to Example 19b starting from 7.15 g (0.029 mol) of 5-methoxy-2-[2-nitro-ethylidenamino]-benzoic acid (Example 44e), 32 ml acetic anhydride, and 3.52 g (0.035 mol) potassium acetate. The title compound which precipitates from the solution, is filtered off, washed with acetic acid, and dried overnight at 85° C. mp: 278-281° C.; MS: 221 (M++1); HPLC: tret=10.23 min (Grad 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07998972B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-2bca83bda8f645348400e782d9696b07 |
| Source note | uspto-grants-2011_08 |