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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 985683Generated: October 28, 2026

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

https://huagongshe.com/reaction/985683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantMethyl (2S)-2-(2,3,4-trifluoroanilino)propionateHCID 10125210—
Solventtert-Butyl methyl etherHCID 15413—
Product(2S)-2-(2,3,4-Trifluoroanilino)propanolHCID 11401466—

Reaction Steps

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06872823B1
Source datasetuspto-grants-2005_03
ORD IDord-5c40f792b4d145b69411b4c8b6d67627
Source noteuspto-grants-2005_03