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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11455Generated: October 25, 2026

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

https://huagongshe.com/reaction/11455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIsobutyronitrileHCID 6559—
ReactantDiisopropylamineHCID 7912—
ReactantTetrahydrofuranHCID 8028—
ReactantButyllithiumHCID 178418339—
SolventHexaneHCID 8058—
Product3-Hydroxy-2,2-dimethyl-3-(4-pyridyl)propionitrileHCID 1113765671.6%

Reaction Conditions

Temperature-78 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07098226B2
Source datasetuspto-grants-2006_08
ORD IDord-d0983ff7c02048699ba7f9023a7fbbfa
Source noteuspto-grants-2006_08