Dimethyl Sulfoxide → 1-[2-(Tert-butyldimethylsilanyloxy)ethoxy]-3-buten-2-ol

温度

-78 °C

A solution of oxalyl chloride (8.38 mL) in dichloromethane (470 mL) was cooled to −78° C. in a nitrogen atmosphere. A solution of dimethyl sulfoxide (8.01 mL) in dichloromethane (10 mL) was added dropwise to the reaction solution at the same temperature. The reaction solution was stirred at the same temperature for 10 minutes. A solution of 2-[2-(tert-butyldimethylsilanyloxy)ethoxy]ethanol (25.9 g) in dichloromethane (20 mL) was added dropwise to the reaction solution at the same temperature. The reaction solution was stirred at the same temperature for 30 minutes. Triethylamine (52.1 mL) was added to the reaction solution at the same temperature. The reaction solution was stirred for one hour while gradually returning to room temperature. Aqueous ammonium chloride was added to the reaction solution, and the organic layer was separated. The organic layer was washed with saturated aqueous sodium chloride and dried over anhydrous magnesium sulfate. The organic layer was filtered through a silica pad and the filtrate was concentrated. Tetrahydrofuran (500 mL) was added to the residue. The reaction solution was cooled to −78° C. in a nitrogen atmosphere. Vinylmagnesium chloride (148 mL, 1.38 M solution in tetrahydrofuran) was added dropwise to the reaction solution at the same temperature. The reaction solution was heated to room temperature with stirring over six hours. Aqueous ammonium chloride and ethyl acetate were added to the reaction solution, and the organic layer was separated. The organic layer was washed with saturated aqueous sodium chloride and dried over anhydrous magnesium sulfate. The organic layer was concentrated under reduced pressure. The residue was purified by silica gel column chromatography to obtain the title compound (10.03 g).

1. stirringThe reaction solution was stirred at the same temperature for 30 minutes
2. stirringThe reaction solution was stirred for one hour
3. customwhile gradually returning to room temperature
4. customthe organic layer was separated
5. washThe organic layer was washed with saturated aqueous sodium chloride
6. dry with materialdried over anhydrous magnesium sulfate
7. filtrationThe organic layer was filtered through a silica pad
8. concentrationthe filtrate was concentrated
9. additionTetrahydrofuran (500 mL) was added to the residue
10. additionVinylmagnesium chloride (148 mL, 1.38 M solution in tetrahydrofuran) was added dropwise to the reaction solution at the same temperature
11. temperatureThe reaction solution was heated to room temperature
12. stirringwith stirring over six hours
13. additionAqueous ammonium chloride and ethyl acetate were added to the reaction solution
14. customthe organic layer was separated
15. washThe organic layer was washed with saturated aqueous sodium chloride
16. dry with materialdried over anhydrous magnesium sulfate
17. concentrationThe organic layer was concentrated under reduced pressure
18. customThe residue was purified by silica gel column chromatography

ORDレコード

ord-97ae05e239b8460c82ae2f9e6b23fe85

出典データセット

uspto-grants-2012_06

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US08198269B2