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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1696322Erstellt: 25. Oktober 2026

Sodium Sulfite → 3-(1-(Tert-butyldimethylsilyloxy)cyclobutyl)propane-1,2-diol

https://huagongshe.com/reaction/1696322

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium SulfiteHCID 24437—
EduktMethyl morpholine oxideHCID 82029—
Edukt(1-Allylcyclobutoxy)(tert-butyl)dimethylsilaneHCID 66844818—
Edukt2-Methylpropan-2-ol--water (1/1)HCID 71401949—
KatalysatorOsmium TetroxideHCID 30318—
LösungsmittelWaterHCID 962—
Produkt3-(1-(Tert-butyldimethylsilyloxy)cyclobutyl)propane-1,2-diolHCID 66845148—

Reaktionsschritte

To a 2 L round bottomed flask was added (1-allylcyclobutoxy) (tert-butyl)dimethylsilane (previous step) and H2O/t-BuOH (1:1, 1 L). NMO (32.68 g, 279 mmol) was added to the mixture. After stirring for 5 min the solution was found to be homogenous. Osmium tetroxide (1.00 g, 3.93 mmol) was added and the reaction was stirred at RT. After 2 h, TLC revealed the reaction to be complete. 500 mL of H2O and sodium sulfite (19.5 g, 155 mmol) were added and the reaction was stirred for another hour. The aqueous solution was extracted with ether (2×1 L). The combined organics were concentrated in vacuo to give 3-(1-(tert-butyldimethylsilyloxy)cyclobutyl)propane-1,2-diol, as a light yellow oil. The oil contained some t-BuOH, but was carried forward without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08163766B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-7dbd3081f1424549a5625553e636acc7
Quellennotizuspto-grants-2012_04