HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Acetate → HCID 67587774, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 67586747 | HCID 67586747 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 67587774 | HCID 67587774 | — |
Reaction Steps
The compound can be prepared from N-[6-(4-benzoylphenoxy)-hexyl]-maleamic acid from Example 11 by reacting with acetic acid and sodium acetate according to the method described in Example 2. The desired maleimide was isolated as its monohydrate by flash column chromatography. Mp 84--6° C. (Found: C, 72.78; H, 6.28; N, 3.58%. C23H23NO3, H2O requires C, 73.19; H, 6.65; N, 3.69%). H.p.l.c. 100%. FAB ms 378 (MH+). 1H-n.m.r. (CDCl3) δ 6.9 (2H, m, aromatic), 6.6 (2H, d, CH=CH), 3.9 (2H, m, CH2), 3.5 (2H, m, CH2), 1.8 (2H, m, CH2), 1.6 (2H, m, CH2), 1.5 (2H, m, CH2), 1.3 (2H, m, CH2). λmax (CH2Cl2) 286 nm, ε 16590.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05877204 |
| Source dataset | uspto-grants-1999_03 |
| ORD ID | ord-ccd51235399446c5b6cd6e4b302d3bbd |
| Source note | uspto-grants-1999_03 |