HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8464Generated: October 28, 2026
Methanol → (2S)-2-(2,3,4-Trifluoroanilino)propanol
https://huagongshe.com/reaction/8464
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Methyl (2S)-2-(2,3,4-trifluoroanilino)propionate | HCID 10125210 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | (2S)-2-(2,3,4-Trifluoroanilino)propanol | HCID 11401466 | — |
Reaction Steps
At room temperature, sodium borohydride (35.7 mg) was suspended in 1,2-dimethoxyethane (0.2 ml). Then a solution (0.8 ml) of methyl (2S)-2-(2,3,4-trifluoroanilino)propionate (200 mg, 99.8% ee) in DME was added to the solution. After adding methanol (137.4 mg), the liquid reaction mixture was stirred for 1 hour. Then water was added to the liquid reaction mixture followed by extraction with ethyl acetate. The organic layer was washed with water and a saturated aqueous solution of ammonium chloride and dried over anhydrous magnesium sulfate. After evaporating the solvent, the obtained residue was subjected to silica gel column chromatography to thereby give 176 mg (99.8% ee) of the title compound as an oily substance. The 1H-NMR and IR spectral data of this product was identical with those of the compound obtained in Example 51.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07087778B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-ca71e4439f8a46408b5c9887a26e760f |
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| Source note | uspto-grants-2006_08 |
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