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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8466Generated: October 29, 2026

Methanol → (2S)-2-(2,3,4-Trifluoroanilino)propanol

https://huagongshe.com/reaction/8466

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantMethyl (2S)-2-(2,3,4-trifluoroanilino)propionateHCID 10125210—
SolventDichloromethaneHCID 6344—
Product(2S)-2-(2,3,4-Trifluoroanilino)propanolHCID 11401466—

Reaction Steps

At room temperature, sodium borohydride (35.7 mg) was suspended in methylene chloride (0.2 ml). Then a solution (0.8 ml) of methyl (2S)-2-(2,3,4-trifluoroanilino)propionate (200 mg, 99.8% ee) in metylene chloride 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 159.8 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087778B2
Source datasetuspto-grants-2006_08
ORD IDord-29ebbd36a0d347fd8065424702aa0c74
Source noteuspto-grants-2006_08