HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72578Generated: October 25, 2026
5-Bromo-2-chlorobenzaldehyde → (5-Bromo-2-chloro-phenyl)-[1-(4-methoxy-benzyl)-1,2,3,4-tetrahydro-quinolin-6-yl]-methanol
https://huagongshe.com/reaction/72578
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-Bromo-2-chlorobenzaldehyde | HCID 10608925 | — |
| Reactant | 6-Bromo-1-(4-methoxy-benzyl)-1,2,3,4-tetrahydro-quinoline | HCID 58340853 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (5-Bromo-2-chloro-phenyl)-[1-(4-methoxy-benzyl)-1,2,3,4-tetrahydro-quinolin-6-yl]-methanol | HCID 67115847 | 65.1% |
Reaction Steps
To a cooled solution of 6-bromo-1-(4-methoxy-benzyl)-1,2,3,4-tetrahydro-quinoline (2.5 g, 7.5 mmol) in THF (30 mL) was added 1.6 M n-butyl lithium in hexanes (4.7 mL, 7.5 mmol) at −78° C., stirred for 30 min. This was transferred to a stirred solution of 5-bromo-2-chlorobenzaldehyde (1.73 g, 7.9 mmol) in THF (30 mL) at −78° C. After stirring for 30 min, reaction was quenched by the addition of saturated aqueous solution of ammonium chloride and extracted with ethyl acetate (2×50 mL). The ethyl acetate layer was washed with water, brine, dried over sodium sulphate, and concentrated. The resulting residue was purified by silica gel column chromatography to give (5-bromo-2-chloro-phenyl)-[1-(4-methoxy-benzyl)-1,2,3,4-tetrahydro-quinolin-6-yl]-methanol (2.31 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08828951B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-534c33aa1e59440facf12c843a8c0023 |
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| Source note | uspto-grants-2014_09 |
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