HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790199Generated: October 25, 2026
Water → 7-bromo-1,4,4,6-tetramethyl-3,4-dihydro-1H-quinoline-2-one
https://huagongshe.com/reaction/1790199
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| 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 | 104.5% |
Reaction Steps
A mixture of powdered potassium hydroxide (3.35 g, 59.67 mmol) in DMSO (40 mL) was stirred at 0° C. for 10 min. 7-bromo-4,4,6-trimethyl-3,4-dihydro-1H-quinoline-2-one (Example 1e) (8.0 g, 29.83 mmol) was added cautiously, followed immediately by the addition of ethyl iodide (12 mL, 149.17 mmol). 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 8.8 g of 7-bromo-1,4,4,6-tetramethyl-3,4-dihydro-1H-quinoline-2-one and used without further purification in the Suzuki coupling (step a). 1H NMR (300 MHz; CDCl3): 1.24 (t, J=7.2 Hz, 1 H), 1.25 (s, 6 H), 2.37 (s, 3 H), 2.45 (s, 2 H), 3.98 (q, 2 H), 7.13 (s, 1 H), 7.18 (s, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07071218B2 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-77caa91568234d24a077c16a3f1fb4fb |
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| Source note | uspto-grants-2006_07 |
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