Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | HCID 21466811 | HCID 21466811 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 135976857 | HCID 135976857 | 70.6% |
Reaction Steps
To 35 ml of acetic acid, 2.5 g of 6-decyl-2-(4-methoxyphenyl)quinoline and 15 ml of 47%-hydrobromic acid were added, followed by stirring for 12 hours at 100° C. and further stirring overnight at room temperature. After the reaction, the reaction mixture was poured into water and subjected to extraction with chloroform. The organic layer was washed with water and dried with anhydrous sodium sulfate, followed by distilling-off of the solvent and purification by silica gel column chromatography to obtain 1.7 g of 6-decyl-2-(4-hydroxyphenyl)quinoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05695684 |
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| Source dataset | uspto-grants-1997_12 |
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| ORD ID | ord-4e12053d4b024fd6ae6e1fecc0fd0bda |
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| Source note | uspto-grants-1997_12 |
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