HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-[3-(2-chloro-4-methoxyphenoxy)propyloxymethyl]-4-hydroxy-2(1H)-quinolinone → 1-[3-(2-Chloro-4-Methoxyphenoxy)-propoxymethyl]-3-Formyl-4-Hydroxy-2(1H)-Quinolinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-[3-(2-chloro-4-methoxyphenoxy)propyloxymethyl]-4-hydroxy-2(1H)-quinolinone | HCID 54736848 | — |
| Reactant | 2,4-Dihydroxy-3-formylquinoline | HCID 135408807 | — |
| Product | 1-[3-(2-Chloro-4-Methoxyphenoxy)-propoxymethyl]-3-Formyl-4-Hydroxy-2(1H)-Quinolinone | HCID 135786519 | — |
Reaction Steps
Following the procedure set forth in Preparation B, 1-[3-(2-chloro-4-methoxyphenoxy)propyloxymethyl]-4-hydroxy-2(1H)-quinolinone was converted to 1[3-(2-chloro-4-methoxy)phenoxy)propyloxymethyl]-3-formyl-4-hydroxy-2(1H)-quinolinone. That the expected product was obtained was confirmed by the spectral data: MS: m/e 417 (M·+); NMR (CDCl3): δ2.01 (q, 2H, CH2), 3.75 (s, 3H, OCH3), 3.85 (q, 4H, CH2 --O), 10.21 (s, 1H, CHO).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05378694 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-fb5838f0374a425aab56b1ccfba9d7b4 |
| Source note | uspto-grants-1995_01 |