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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1009098Erstellt: 27. Oktober 2026

Methanol → (S)-2,3-bis(tert-butyldimethylsilyloxy)propan-1-ol

https://huagongshe.com/reaction/1009098

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktDiisobutylaluminum hydrideHCID 14487—
EduktPotassium alloy, nonbase, K,NaHCID 16211683—
Edukt(S)-2,3-bis(tert-butyldimethylsilyloxy)propyl 4-methoxybenzoateHCID 44240216—
LösungsmittelDichloromethaneHCID 6344—
Produkt(S)-2,3-bis(tert-butyldimethylsilyloxy)propan-1-olHCID 46201106—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a 1.0 L RB flask containing (S)-2,3-bis(tert-butyldimethylsilyloxy)propyl 4-methoxybenzoate (9.200 g, 20 mmol) was added DCM (100 mL) and the mixture was allowed to stir at −78° C. for 5 minutes. At this time, DIBAL-H (1.0 M, hexanes) (61 ml, 61 mmol) was added via a syringe. The reaction was allowed to stir for 30 min and then quenched with MeOH (4.1 ml, 101 mmol). Sodium potassium tartate (sat, 200 mL) and DCM (100 mL) was added and the solution was allowed to warm to 23° C. and stirred for 3 h. The aq. layer was extracted with DCM (3 100 mL). The combined organics were washed with brine and dried with sodium sulfate and concentrated to give a residue.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07973047B2
Quelldatensatzuspto-grants-2011_07
ORD IDord-ee0171770acb409f844c32297c1eb0f5
Quellennotizuspto-grants-2011_07