HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 737069Generated: October 30, 2026
Toluene → 2-Phenyl-4-(2'-trifluoromethyl-biphenyl-4-ylmethyl)-morpholine
https://huagongshe.com/reaction/737069
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-(Trifluoromethyl)benzeneboronic acid | HCID 2734387 | — |
| Reactant | 4-(4-Bromo-benzyl)-2-phenyl morpholine | HCID 57849504 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Phenyl-4-(2'-trifluoromethyl-biphenyl-4-ylmethyl)-morpholine | HCID 16126849 | 69.6% |
Reaction Steps
106 mg of 4-(4-Bromo-benzyl)-2-phenyl-morpholine was combined with 91 mg of 2-(Trifluoromethyl)phenyl boronic acid, 18 mg of tetrakis(triphenylphosphine)palladium(0), 1.1 mL of 2M sodium carbonate solution, 2.9 mL toluene and 1.4 mL ethanol. The reaction mixture was heated in a sealed tube at 120° C. overnight in an oil bath. The reaction mixture was filtered through Celite and concentrated in vacuo. The residue was diluted with water and extracted with ethyl acetate. The combined organic phases were washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The crude material was purified by flash chromatography eluting in a 10 to 40% ethyl acetate/hexanes gradient. The product fractions were pooled and concentrated to afford 88.3 mg of product. ES MS (+) m/z 398
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07595397B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-e1de05e62a414082b5fe2c464728be32 |
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| Source note | uspto-grants-2009_09 |
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