Boron trifluoride etherate → Silane, trimethyl(3,3,3-triethoxy-1-propynyl)-

温度

-78 °C

Boron trifluoride diethyl etherate (36.0 mL, 280 mmol) was added to diethyl ether (50 mL) under argon. The mixture was transferred to a dropping funnel and added dropwise under argon to a solution of tetraethyl orthocarbonate (40.0 g, 208 mmol) in diethyl ether (100 mL) at 0° C. After the addition was complete, the mixture was stirred for 5 min and then cooled to −78° C. In a separate reaction flask, n-butyllithium (166 mL, 2.5 M solution in hexanes, 416 mmol) was added dropwise to a solution of trimethylsilyl acetylene (59.0 mL, 416 mmol) in diethyl ether (200 mL) at 0° C. under argon. After stirring for 1 h at 0° C., the solution was cooled to −78° C. This solution was added via cannula to the triethoxycarbenium tetrafluoroborate formed previously. The mixture was stirred at −78° C. for 1 h before being warming to room temperature. Saturated aqueous potassium carbonate was added and mixture was extracted with diethyl ether. The organic extracts were dried with magnesium sulfate and the solvent was removed under reduced pressure to give the title compound (50.0 g, 100% yield) as yellow oil. 1H NMR (CDCl3) δ 3.68(q, 6H, J=7.2 Hz), 1.23 (t, 9H, J=7.2 Hz), 0.20, (s, 9H).

1. customThe mixture was transferred to a dropping funnel
2. additionAfter the addition
3. stirringAfter stirring for 1 h at 0° C.
4. temperaturethe solution was cooled to −78° C
5. customformed previously
6. stirringThe mixture was stirred at −78° C. for 1 h
7. temperaturebefore being warming to room temperature
8. extractionmixture was extracted with diethyl ether
9. dry with materialThe organic extracts were dried with magnesium sulfate
10. customthe solvent was removed under reduced pressure

ORDレコード

ord-fb683411844248e3bb87cff62d458c50

出典データセット

uspto-grants-2005_02

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US06855722B2