HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258870Generated: October 26, 2026
Benzyl Bromide → N-benzyl-7-bromo-1,2,3,4-tetrahydroquinoline
https://huagongshe.com/reaction/1258870
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 7-Bromo-1,2,3,4-tetrahydroquinoline | HCID 13865047 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-benzyl-7-bromo-1,2,3,4-tetrahydroquinoline | HCID 46894871 | 71.2% |
Reaction Steps
To a stirred solution of 7-bromo-1,2,3,4-tetrahydroquinoline (7.0 g, 33.0 mmol) in DMF (50 mL) was added potassium carbonate (13.6 g, 99.0 mmol), and benzyl bromide (4.33 mL, 36.3 mmol), and the mixture was heated to 60° C. for 12 h, then cooled to room temperature and quenched by the addition of ice-cold water (150 mL). The resulting mixture was extracted with ethyl acetate (3×50 mL), and the organic layers were combined and washed with water (50 mL) and brine (50 mL), then dried over sodium sulfate, concentrated and purified by silica gel column chromatography to furnish 1-benzyl-7-bromo-1,2,3,4-tetrahydro-quinoline (7.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08466114B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-06cc487a1729405b8693c02686b23b19 |
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| Source note | uspto-grants-2013_06 |
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