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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1894911Erstellt: 25. Oktober 2026

Pinacolone → 5-Hydroxy-2,2,6,6-tetramethyl-3-heptanone

https://huagongshe.com/reaction/1894911

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPinacoloneHCID 6416—
EduktHexaneHCID 8058—
EduktPivalaldehydeHCID 12417—
EduktLithium diisopropylamideHCID 2724682—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-Hydroxy-2,2,6,6-tetramethyl-3-heptanoneHCID 1097621095%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a solution of pinacolone (10 g, 100 mmol, 1), in anhydrous THF (500 mL), at −78° C. a 2.0 M solution of lithium diisopropylamide (LDA) in hexane (60 mL, 120 mmol) over a period of 30 min. The reaction was stirred at −78° C. for another 30 min. To the resulting white suspension pivalaldehyde (10.9 mL, 100 mmol) was added drop-wise via syringe and the reaction continued for another 12 hrs at room temperature. The reaction was quenched by adding 10 mL of water. Approximately 80% THF was removed and the mixture was then poured into saturated aqueous solution of NH4Cl. The aqueous layer was extracted twice with diethyl ether (200 mL) and the organic layer was washed with plenty of water. The organic layer was then dried over MgSO4 and concentrated to give a crude yellow solid of β-hydroxy ketone (17.2 g, 95%, (2)). The crude product was recrystallized from hexane to give pure white solid with a yield of 81%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08513377B2
Quelldatensatzuspto-grants-2013_08
ORD IDord-d6685dcad89e4739b31b18f835ca803b
Quellennotizuspto-grants-2013_08