HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 6-Bromo-3,4-dihydro-4-methyl-2(1H)-quinolinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 4-methyl-3,4-dihydro-1H-quinolin-2-one | HCID 5246148 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 6-Bromo-3,4-dihydro-4-methyl-2(1H)-quinolinone | HCID 20158974 | — |
Reaction Steps
A solution of bromine (0.08 cm3) in acetic acid (1 cm3) was added at room temperature to a stirred solution of 4-methyl-3,4-dihydro-2-(1H)-quinolone (0.5 g) in acetic acid (4.0 cm3). After 2 hours, volatile material was removed in vacuo, the residue was partitioned between chloroform (50 cm3) and water (20 cm3), and the organic phase was further extracted with chloroform (2×20 cm3). The combined and dried (MgSO4) organic extracts were evaporated in vacuo and the solid residue was recrystallised from ethyl acetate to afford 6-bromo-4-methyl-3,4-dihydro-2-(1H)-quinolone, m.p. 190°, (0.35 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04710507 |
| Source dataset | uspto-grants-1987_12 |
| ORD ID | ord-7553d1d884034a6e93dc5b31500d4c53 |
| Source note | uspto-grants-1987_12 |