HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944075Generated: October 26, 2026
Sodium Iodide → 6-Bromo-1-(4-methoxy-benzyl)-1,2,3,4-tetrahydro-quinoline
https://huagongshe.com/reaction/1944075
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Methyloxybenzyl chloride | HCID 69993 | — |
| Reactant | 6-Bromo-1,2,3,4-tetrahydroquinoline | HCID 4715029 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Bromo-1-(4-methoxy-benzyl)-1,2,3,4-tetrahydro-quinoline | HCID 58340853 | 62.2% |
Reaction Steps
To a stirred solution of 6-bromo-1,2,3,4-tetrahydro-quinoline (3.00 g, 12.1 mmol) in dimethylformamide (25 ml) was added potassium carbonate (3.3 g, 24.1 mmol), sodium iodide (0.905 g, 6.0 mmol) and 4-methoxybenzyl chloride (2.5 ml, 18.1 mmol) and heated at 50° C. After 18 h, reaction mixture was cooled to room temperature and quenched by the addition of water and extracted with ethyl acetate (2×20 ml). The organic layer was washed with water (2×20 mL), brine (20 mL), dried over sodium sulfate, concentrated and purified by the silica gel column chromatography to furnish 6-bromo-1-(4-methoxy-benzyl)-1,2,3,4-tetrahydro-quinoline (2.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08394772B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-ebde4235801b441dadcca826684b0cb0 |
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| Source note | uspto-grants-2013_03 |
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