Phenol → (2S)-1-chloro-3-phenoxypropan-2-ol

Participants

Reaction Steps

To a mixture of N′,N′-disalicylidene ethylenediaminatocobalt(II) (138 mg, 0.425 mmol) and dichloromethane (10 ml) was added methanesulfonic acid (3 μl, 0.510 mmol) and the reaction system was stirred for 1 hour while being filled with air. The reaction solution was evaporated to dryness under reduced pressure to give a crude blackish (dark) brown cobalt (III) complex. Thereto was added tert-butylmethyl ether (4 ml) to disperse the crude cobalt (III) complex and then thereto were added (S)-epichlorohydrin (2.00 ml, 25.5 mmol, optical purity 99% e.e.) and phenol (2.00 g, 21.3 mmol) in order. The mixture was stirred for 24 hours under nitrogen atmosphere at room temperature. After the reaction, the reaction mixture was diluted with tert-butylmethyl ether (20 ml), the solution was washed with a 6% aqueous sodium hydroxide solution (10 ml) and a saturated sodium chloride solution (10 ml) in order, and the organic layer was condensed under reduced pressure to give crude (S)-1-chloro-3-phenoxy-2-propanol (4.85 g). This crude compound (4.85 g) was dissolved in isopropanol (10 ml) and thereto was added a 24% aqueous sodium hydroxide solution (4.50 g, 25.5 mmol) under ice-cooling. The mixture was stirred for 1 hour at room temperature. After the reaction, the reaction mixture was diluted with tert-butylmethyl ether (50 ml) and the solution was washed with water (20 ml), a saturated aqueous ammonium solution (20 ml) and a saturated aqueous sodium chloride solution (20 ml) in order. The organic layer was condensed under reduced pressure to give crude (R)-glycidylphenyl ether (3.24 g). Quantitative analysis by gas chromatography and optical purity measurement by HLPC were conducted on the compound. As a result the subject compound, (R)-glycidylphenyl ether (3.07 g, 96.1%) was produced with optical purity at. 99% e.e.

Provenance & Evidence