HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582106Generated: October 26, 2026
3,5-Bis(trifluoromethyl)benzoyl chloride → 2-(R)-(3,5-Bis(trifluoromethyl)benzoyloxy)-3-(S)-phenyl-4-benzyl Morpholine
https://huagongshe.com/reaction/582106
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,5-Bis(trifluoromethyl)benzoyl chloride | HCID 101856 | — |
| Reactant | Lithium tri-s-butylborohydride | HCID 3611392 | — |
| Reactant | (3S)-4-Benzyl-3-phenylmorpholin-2-one | HCID 15871960 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(R)-(3,5-Bis(trifluoromethyl)benzoyloxy)-3-(S)-phenyl-4-benzyl Morpholine | HCID 10529667 | 80% |
Reaction Steps
A solution of 2.67 g (10.0 mmol) of 3-(S)-phenyl-4-benzyl-2-morpholinone (from Example 14) in 40 mL of dry THF was cooled to -78° C. The cold solution was treated with 12.5 mL of 1.0M L-Selectride®, solution in THF, maintaining the internal reaction temperature below -70° C. The resulting solution was stirred cold for 45 minutes and the reaction was charged with 3.60 mL (20.0 mmol) of 3,5-bis(trifluoro-methyl)benzoyl chloride. The resulting yellow mixture was stirred cold for 30 minutes and the reaction was quenched with 50 mL of saturated aqueous sodium bicarbonate solution. The quenched mixture was partitioned between 300 mL of ether and 50 mL of water and the layers were separated. The organic layer was dried over magnesium sulfate. The aqueous layer was extracted with 300 mL of ether; the extract was dried and combined with the original organic layer. The combined organics were concentrated in vacuo. Flash chromatography on 150 g of silica gel using 37:3 v/v hexanes/ether as the eluant afforded 4.06 g (80%) of the title compound as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05922706 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-551c1aab1b984440b77fc65f5c3a1393 |
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| Source note | uspto-grants-1999_07 |
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