Phenol → HCID 9794095, compound

To a mixture of N′,N′-disalicylidene ethylenediaminatocobalt(II) (173 mg, 0.532 mmol) and dichloromethane (13 ml) was added (±) camphorsulfonic acid (148 mg, 0.638 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 (5 ml) to disperse the crude cobalt (III) complex and then thereto were added (R)-epichlorohydrin (2.50 ml, 31.9 mmol, optical purity 99% e.e.) and phenol (2.50 g, 26.6 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 (R)-1-chloro-3-phenoxy-2-propanol (5.44 g). This crude compound (5.44 g) was dissolved in isopropanol (10 ml) and thereto was added a 24% aqueous sodium hydroxide solution (6.64 g, 39.8 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 (2.0 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 (S)-glycidylphenyl ether (3.80 g). Quantitative analysis by gas chromatography and optical purity measurement by HLPC were conducted on the compound. As a result the subject compound, (S)-glycidylphenyl ether (3.71 g, 93.0%) was produced with optical purity at 99% e.e.

1. additionwhile being filled with air
2. customThe reaction solution was evaporated to dryness under reduced pressure
3. customto give a crude blackish (dark) brown cobalt (III) complex
4. additionto disperse the crude cobalt (III) complex
5. stirringThe mixture was stirred for 24 hours under nitrogen atmosphere at room temperature
6. customAfter the reaction
7. washthe solution was washed with a 6% aqueous sodium hydroxide solution (10 ml)
8. customcondensed under reduced pressure

ORD record

ord-814fe967cd7e4e7e934626dc7725cdb3

Source dataset

uspto-grants-2005_09

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06946566B2