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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1393159Erstellt: 26. Oktober 2026

Water → 3-Hydroxy-2,2-dimethyl-3-(4-pyridyl)propionitrile

https://huagongshe.com/reaction/1393159

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktIsobutyronitrileHCID 6559—
EduktDiisopropylamineHCID 7912—
EduktTetrahydrofuranHCID 8028—
EduktButyllithiumHCID 178418339—
LösungsmittelHexaneHCID 8058—
Produkt3-Hydroxy-2,2-dimethyl-3-(4-pyridyl)propionitrileHCID 1113765671,6%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

A solution of diisopropylamine (10.0 ml, 71.5 mmol) in tetrahydrofuran (150 ml) was cooled to −78° C. under a nitrogen atmosphere, and a 1.6 N solution of butyllithium in hexane was added dropwise thereto over 10 minutes. The mixture was cooled with ice-cold water for 20 minutes and then cooled to −78° C. again, and isobutyronitrile (3.03 ml, 33.3 mmol) was added dropwise to the mixture over five minutes. Further, 4-pyridinecarboxyaldehyde (3.18 ml, 33.3 mmol) was added dropwise thereto over five minutes, and the whole was stirred for one hour 20 minutes. Water (100 ml) was added to the reaction mixture, and the whole was extracted with ethyl acetate (200 ml) by using a continuous extracting apparatus for three days. The obtained organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting solid was filtered off with diethyl ether to give 4.20 g (71.6%) of 3-hydroxy-2,2-dimethyl-3-(4-pyridyl)propionitrile as a colorless solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07345064B2
Quelldatensatzuspto-grants-2008_03
ORD IDord-5e6bacc9311e4ebc83b58c8f4a3c7cb6
Quellennotizuspto-grants-2008_03