Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 3-Bromo-4-chloroquinoline | HCID 618306 | — |
| Product | HCID 14209239 | HCID 14209239 | — |
Reaction Steps
A mixture of 3 g of 3-bromo-4-chloro-quinoline and 10 g of aminopropanol-2 was heated to 150° C. for 20 minutes. The mixture was cooled and poured into 120 ml of water and the product was extracted with 100 ml of ether. The ether layer was dried over sodium sulfate, the solvent removed by evaporation and the residue recrystallized from ether/hexane. The yield was 2.6 g, mp 82°-83° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04942168 |
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| Source dataset | uspto-grants-1990_07 |
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| ORD ID | ord-b8c72af5dfe94e909c32c79ff633b60d |
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| Source note | uspto-grants-1990_07 |
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