HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782680Generated: October 30, 2026
3-Bromobenzyl bromide → 1-(3-Bromo-benzyl)-7-trifluoromethyl-1,2,3,4-tetrahydro-quinoline
https://huagongshe.com/reaction/1782680
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Bromobenzyl bromide | HCID 69979 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 7-(Trifluoromethyl)-1,2,3,4-tetrahydroquinoline | HCID 2781139 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(3-Bromo-benzyl)-7-trifluoromethyl-1,2,3,4-tetrahydro-quinoline | HCID 11595823 | 82% |
Reaction Steps
Under a nitrogen atmosphere, a solution of bromo-3-bromomethyl-benzene (3.47 g, 13.p mmol) and 7-trifluoromethyl-1,2,3,4-tetrahydro-quinoline (2.93 g, 14.6 mmol) in ethanol (15 mL, 1 M) was treated with sodium acetate (5.69 g, 69.3 mmol) and heated to 80° C. After stirring 2 h, the solution was cooled to room temperature, diluted with water, extracted with ethyl acetate and washed with saturated aq sodium chloride. The organic layer was dried over MgSO4, filtered and concentrated. Purification by column chromatography (10% ethyl acetate in heptane) provided 1-(3-bromo-benzyl)-7-trifluoromethyl-1,2,3,4-tetrahydro-quinoline 4.21 g (82%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07498356B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-b2cd2207d0084987a974d1c5932b137e |
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| Source note | uspto-grants-2009_03 |
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