Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1183962Erstellt: 27. Oktober 2026

Sodium borohydride → 3-(2-{[Tert-butyl(diphenyl)silyl]oxy}ethyl)cyclobutanol

https://huagongshe.com/reaction/1183962

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium borohydrideHCID 4311764—
Edukt3-(2-{[Tert-butyl(diphenyl)silyl]oxy}ethyl)cyclobutanoneHCID 57565772—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-(2-{[Tert-butyl(diphenyl)silyl]oxy}ethyl)cyclobutanolHCID 5756574569,6%

Reaktionsschritte

3-(2-{[Tert-butyl(diphenyl)silyl]oxy}ethyl)cyclobutanone (5.11 g, 14.5 mmol) (WO 2006063281) was dissolved in tetrahydrofuran (120 mL). Sodium borohydride (548 mg, 14.5 mmol) was added and the reaction was stirred overnight at room temperature. The reaction was quenched with water and saturated aqueous sodium bicarbonate and stirred for 20 min until the bubbling ceased. The reaction mixture was diluted with ether and the aqueous layer was extracted with ether. The combined organic layers were washed with brine, dried over magnesium sulfate, filtered and evaporated in vacuo to give 3-(2-{[tert-butyl(diphenyl)silyl]oxy}ethyl)cyclobutanol (3.58 g, 69.6%) as a clear oil. Partial 1H NMR indicated a ˜3.5:1 mix of cis-trans isomers. (CDCl3, δ ppm, key peaks are 4.08 (quintet, J=7.42, 0.78H) and 4.34 (quintet, J=6.83, 0.22H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08664401B2
Quelldatensatzuspto-grants-2014_03
ORD IDord-d182d90039e64e1aa36935a568663b28
Quellennotizuspto-grants-2014_03