tert-Butyl hydroperoxide → (2S,3S)-3-((Phenylmethoxy)methyl)-2-oxiranemethanol

温度

-23 °C

3.3 g of molecular sieve (powder, 3A) was suspended in 190 ml of dry dichloromethane, and 4.2 ml of isopropyl orthotitanate and 2.9 ml of diethyl L(+)-tartrate were added thereto at -23° C. under stirring. 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-butylhydroperoxide (a 5.17M dichloromethane solution) was added thereto, and the mixture was stirred for further 7 hours. Then, the reaction mixture was left to stand at -23° C. overnight. 190 ml of diethyl ether and 4.2 ml of a saturated sodium sulfate aqueous solution were added to the reaction solution, and the mixture was stirred at room temperature for 4 hours. Insolubles were removed by filtration, and then the solvent was distilled off under reduced pressure. The residue was dissolved in 240 ml of diethyl ether. 42 ml of a 1N sodium hydroxide aqueous solution was added thereto at 0° C. under stirring, and the mixture was stirred at 0° C. for 30 minutes. The ether layer was washed sequentially with a saturated sodium hydrogencarbonate aqueous solution and with 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 7 hours
4. waitThen, the reaction mixture was left
5. stirringthe mixture was stirred at room temperature for 4 hours
6. customInsolubles 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. stirringat 0° C. under stirring
11. stirringthe mixture was stirred at 0° C. for 30 minutes
12. washThe ether layer was washed sequentially with a saturated sodium hydrogencarbonate aqueous solution and with a saturated sodium chloride aqueous solution
13. dry with materialdried 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-ae93bd540cac49d088834834137478d3

出典データセット

uspto-grants-1995_06

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US05424309