HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromohexane → 2-Hydroxyquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromohexane | HCID 8101 | — |
| Reactant | Isatoic Anhydride | HCID 8359 | — |
| Product | 2-Hydroxyquinoline | HCID 6038 | — |
Reaction Steps
Following the procedure set forth in Steps (2) to (4) of Preparation A, isatoic anhydride was reacted with hexyl bromide to give 1-hexyl-4-hydroxy-(2(1H)-quinolinone. That the expected product was obtained was confirmed by the spectral data: MS: role 245 (M·+); NMR (DMSO): δ0.9 (t, 3H, CH3 --CH2 --), 4.06 (t, 2H, N--OH2), 6.18 (s, 1H, =CH), 11.87 (br, 1H, OH) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05378694 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-3618e82ea889410eb8880cde70794958 |
| Source note | uspto-grants-1995_01 |