HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898823Generated: October 30, 2026
4-(Trifluoromethyl)aniline → HCID 11301521, compound
https://huagongshe.com/reaction/898823
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(Trifluoromethyl)aniline | HCID 9964 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 5365845 | HCID 5365845 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 11301521 | HCID 11301521 | 75.3% |
Reaction Steps
To a solution of 4-trifluoromethylaniline (193 mg, 1.2 mmol) and 3-crotonoyl-1,3-oxazolidin-2-one (155 mg, 1.0 mmol) in toluene (3 ml) in a stream of nitrogen was added Pd((R)-binap)(H2O)2(OTf)2 (26.6 mg, 0.025 mmol) and the resulting mixture was stirred at room temperature for 16 hours. After completion of the reaction, a saturated aqueous solution of ammonium chloride (10 ml) was added to the reaction mixture and the resulting mixture was extracted with ethyl acetate (10 ml). The organic layer was dried over anhydrous magnesium sulfate. The solvent was then evaporated off and the crude product obtained was purified by a silica gel column chromatography (hexane:ethyl acetate=1:1) to give the objective compound 3-(4-trifluoromethylanilino)butyryl-1,3-oxazolidin-2-one (238 mg, 75% yield). Enantiomeric excess ratio of this product was determined by a liquid chromatography using a column for separation of optical isomers (column: AD-H) to be 83% e.e.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07351849B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-c2539e421c084425899c51982ee7f755 |
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| Source note | uspto-grants-2008_04 |
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