HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503825Generated: October 26, 2026
Water → 7-(4-bromobutoxy)-3,4-dihydro-2(1H)-quinolinone
https://huagongshe.com/reaction/503825
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 1,4-Dibromobutane | HCID 8056 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 7-Hydroxy-3,4-dihydrocarbostyril | HCID 2785758 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 7-(4-bromobutoxy)-3,4-dihydro-2(1H)-quinolinone | HCID 10542064 | — |
Reaction Steps
1,4-dibromo butane (509 ml) was added to a stirred solution of 7-hydroxy-3,4-dihydrocarbostyril (100 gm) in dimethylacetamide (500 ml) at ambient temperature. The reaction mixture was heated at 36° to 40° C. Sodium hydroxide (33.1 gm) was added to the reaction mixture at the interval of 30 min (Complete the addition of sodium hydroxide in 9 equal fractions in 4.0 hours). The reaction mixture was cooled at ambient temperature and D.M Water was added to it. The reaction mixture was extracted with ethylacetate. Organic layer was separated and washed with 5% brine and finally dried over sodium sulphate. The organic layer was evaporated to dryness under reduced pressure (10 mm) at 45° C. to obtain residue. To the residue cyclohexane (1000 ml) was added to give of 7-(4-bromobutoxy)-3,4-dihydrocarbostyril.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07777039B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-a2ac5476bbdb4390a7c999ce2e318aa0 |
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| Source note | uspto-grants-2010_08 |
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