HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790195Generated: October 25, 2026
Water → 7-bromo-1,4,4,6-tetramethyl-3,4-dihydro-1H-quinoline-2-one
https://huagongshe.com/reaction/1790195
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 7-Bromo-4,4,6-trimethyl-3,4-dihydro-1H-quinoline-2-one | HCID 21966423 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 7-bromo-1,4,4,6-tetramethyl-3,4-dihydro-1H-quinoline-2-one | HCID 21966429 | 101.3% |
Reaction Steps
A mixture of powdered KOH (14.06 g, 0.250 mol) in DMSO (150 mL) was stirred at 0° C. for 10 min. 7-Bromo-4,4,6-trimethyl-3,4-dihydro-1H-quinoline-2-one (33.59 g, 0.125 mol) was added cautiously, followed immediately by the addition of methyl iodide (39 mL, 0.625 mol). The reaction mixture was kept at 0° C. for 30 min then slowly warmed up to room temperature and stirred overnight at room temperature. The reaction mixture was poured into water and extracted with dichloromethane washed with water and brine, dried (Mg2SO4), filtered and evaporated to give 35.74 g of 7-bromo-1,4,4,6-tetramethyl-3,4-dihydro-1H-quinoline-2-one (99%) and used without further purification in the Suzuki coupling (step a). 1H NMR (300 MHz; CDCl3): 1.27 (s, 6 H), 2.37 (s, 3 H), 2.48 (s, 2 H), 3.35 (s, 3 H), 7.12 (s, 1 H), 7.16 (s, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07071218B2 |
|---|
| Source dataset | uspto-grants-2006_07 |
|---|
| ORD ID | ord-4b65c66c2fa4497087cd2562941f4a17 |
|---|
| Source note | uspto-grants-2006_07 |
|---|