Sodium Sulfate → (2S,3S)-3-((Phenylmethoxy)methyl)-2-oxiranemethanol

温度

-23 °C

In 190 ml of dry dichloromethane, 3.3 g of a molecular sieves (powder, 3A) was suspended, and 4.2 ml of isopropyl orthotitanate and 2.9 ml of diethyl L(+)-tartarate were added thereto under stirring at -23° C. The mixture was stirred at the same temperature for 15 minutes. Then, 3 ml of a dry dichloromethane solution of 4.7 g of (E)-4-benzyloxy-2-buten-1-ol was added thereto, and the mixture was stirred at the same temperature for 5 minutes. 11 ml of tert-butylhydroxyperoxide (5.17M dichloromethane solution) was added thereto, and the mixture was stirred for further seven hours. Then, the reaction solution was left to stand at -23° C. overnight. To the reaction solution, 190 ml of diethyl ether and 4.2 ml of a saturated sodium sulfate aqueous solution were added, and the mixture was stirred at room temperature for 4 hours. The insolubles were removed by filtration, and the solvent was distilled off under reduced pressure. The residue was dissolved in 240 ml of diethyl ether, and 42 ml of a 1N sodium hydroxide aqueous solution was added thereto under stirring at 0° C. The mixture was stirred at 0° C. for 30 minutes. The diethyl ether layer was washed sequentially with a saturated sodium hydrogencarbonate aqueous solution and a saturated sodium chloride aqueous solution and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and then the residue was purified by silica gel column chromatography (n-hexane/ethyl acetate=1/1) to obtain 2.9 g of (2S,3S)-4-benzyloxy-2,3-epoxy-1-butanol as colorless oily substance.

1. stirringThe mixture was stirred at the same temperature for 15 minutes
2. stirringthe mixture was stirred at the same temperature for 5 minutes
3. stirringthe mixture was stirred for further seven hours
4. waitThen, the reaction solution was left
5. stirringthe mixture was stirred at room temperature for 4 hours
6. customThe insolubles were removed by filtration
7. distillationthe solvent was distilled off under reduced pressure
8. dissolutionThe residue was dissolved in 240 ml of diethyl ether
9. addition42 ml of a 1N sodium hydroxide aqueous solution was added
10. stirringunder stirring at 0° C
11. stirringThe mixture was stirred at 0° C. for 30 minutes
12. washThe diethyl ether layer was washed sequentially with a saturated sodium hydrogencarbonate aqueous solution
13. dry with materiala saturated sodium chloride aqueous solution and then dried over anhydrous sodium sulfate
14. distillationThe solvent was distilled off under reduced pressure
15. customthe residue was purified by silica gel column chromatography (n-hexane/ethyl acetate=1/1)

ORDレコード

ord-a6da90ea810646c7b13065fc3581c3a9

出典データセット

uspto-grants-1992_06

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US05122523