HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453646Generated: October 31, 2026
Sodium hydride → 4-(3-Bromo-5-methoxy-benzyl)-3,4-dihydro-1H-quinoline-2-one
https://huagongshe.com/reaction/1453646
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Hydrocarbostyril | HCID 64796 | — |
| Reactant | 1-Bromo-3-(bromomethyl)-5-methoxybenzene | HCID 12276449 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(3-Bromo-5-methoxy-benzyl)-3,4-dihydro-1H-quinoline-2-one | HCID 22324259 | — |
Reaction Steps
3,4-Dihydro-2(1H)-quinolinone was purchased from Aldrich Chemical Co. (Cat. No. 41,593-6) and used without purification in this step. 0.45 grams of 3,4-dihydro-2(1H)-quinolinone (3.0 mmole) was dissolved in 15 ml dimethylformamide and cooled in an ice bath. 0.2 grams (4.5 mmole) of sodium hydride (60% wt. in oil ) was added to this solution, and after 5 minutes 0.84 grams 3-bromo-5-methoxy-benzylbromide (3 mmol) was added thereto all at once. The mixture was stirred at ice bath temperature for 1 hour and then quenched by addition of 1% hydrochloric acid. The reaction mix was extracted with ethyl acetate, which was evaporated under reduced pressure to give an oil, which was chromatographed with medium pressure eluting using 10% ethyl acetate in hexanes to yield 0.8 grams of solid 4-(3-bromo-5-methoxy-benzyl)-3,4-dihydro-1H-quinoline-2-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07476675B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-a0bf169bfbea47dbbb490f8183a65566 |
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| Source note | uspto-grants-2009_01 |
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