Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Broxyquinoline | HCID 2453 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-Bromoethanol | HCID 10898 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 11186570 | HCID 11186570 | 76.9% |
Reaction Steps
A solution of 3.79 g of 5,7-dibromo-8-hydroxyquinoline (12.5 mmol) and 975 mL of 2-bromoethanol (13.75 mmol) in 20 mL of dry dimethylformamide containing 5.18 g anhydrous potassium carbonate (37.5 mmol) was placed under argon atmosphere and heated at 60° C. with vigorous magnetic stirring. After 4 hr a further 220 μL of 2-bromoethanol was added and stirring continued at 60° overnight. After 22 hr another 440 μL of 2-bromoethanol was added. After 4 days the mixture was poured into 150 mL of water while stirring. The precipitated product was collected by filtration, washed with 50 mL of 0.5 M aqueous potassium carbonate, plain water and air dried. The solid was washed through the funnel by dissolving in dichloromethane, and the solvent was removed to yield 3.18 g of 5,7-dibromo-8-(2-hydroxyethyl)quinoline. After recrystallization from methanol/water containing a little triethylamine, the melting point was 128–131° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07157408B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-52f211993ca149568dcb695dfebbb221 |
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| Source note | uspto-grants-2007_01 |
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