HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651681Generated: November 1, 2026
Hydrogen Bromide → 7-Bromomethyl-4-chloroquinoline
https://huagongshe.com/reaction/651681
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (4-Chloroquinolin-7-yl)methanol | HCID 22054610 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7-Bromomethyl-4-chloroquinoline | HCID 21708444 | — |
Reaction Steps
7-Hydroxymethyl-4-chloroquinoline (0.2 g, 0.97 mmol) is treated with 48% HBr and heated to 120° C. for 1 h. The resulting solution is cooled with ice, diluted with water and treated with ethyl acetate and sodium bicarbonate until basic to pH paper. The layers are separated and the organic layer is washed with water, dried (Na2SO4) and concentrated to give 7-Bromomethyl-4-chloroquinoline (0.23 g, 0.9 mmol). MS m/z: M+=255; 1H NMR (CDCl3, 300 MHz) δ8.75 (d, 1H), 8.1 (s, 1H), 7.7 (d, 1H), 7.5 (d, 1H), 4.7 (s. 2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06281227B1 |
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| Source dataset | uspto-grants-2001_08 |
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| ORD ID | ord-e0c0649888e84597b30206ed31dbb3e1 |
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| Source note | uspto-grants-2001_08 |
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