HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571780Generated: October 31, 2026
N-Methoxy-N-methyl-3-(trifluoromethyl)benzamide → [4-(4-Benzyl-morpholin-2-yl)-phenyl]-(3-trifluoromethyl-phenyl)-methanone
https://huagongshe.com/reaction/571780
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Methoxy-N-methyl-3-(trifluoromethyl)benzamide | HCID 14069349 | — |
| Reactant | 4-Benzyl-2-(4-bromo-phenyl)-morpholine | HCID 58097879 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [4-(4-Benzyl-morpholin-2-yl)-phenyl]-(3-trifluoromethyl-phenyl)-methanone | HCID 66653802 | 34.6% |
Reaction Steps
To a solution of 4-benzyl-2-(4-bromo-phenyl)-morpholine (1.89 g, 5.7 mmol) in THF (30 mL), at −78° C., was added dropwise n-butyl lithium (2.85 mL; 2.5 mol/l in hexanes; 7.1 mmol). The mixture was stirred for 20 min. at −78° C., and subsequently N-Methoxy-N-methyl-3-trifluoromethyl-benzamide (2.66 g, 11.4 mmol) was added. The mixture was allowed to warm to RT and stirred overnight. The resulting mixture was partitioned between an aqueous saturated NH4Cl solution and EtOAc. The layers were separated. The organic layer was washed with a saturated aqueous NaHCO3-solution, dried (Na2SO4), filtered and concentrated in vacuo. The residue was purified by column chromatography (EtOAc:heptanes 1:3) to afford [4-(4-benzyl-morpholin-2-yl)-phenyl]-(3-trifluoromethyl-phenyl)-methanone (0.84 g), which was used as such in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029371B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-524c2a0f7b4c41079c120d05098835de |
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| Source note | uspto-grants-2015_05 |
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