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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905071Generated: October 31, 2026

Isobutyraldehyde → 4-Formyl-4-methylvaleronitrile

https://huagongshe.com/reaction/1905071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyraldehydeHCID 6561—
ReactantAcrylonitrileHCID 7855—
ReactantSodium HydroxideHCID 14798—
CatalystHydroquinoneHCID 785—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product4-Formyl-4-methylvaleronitrileHCID 8023148,042.199%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of 64.8 g (0.898 mmol, 51.45 mL) of isobutyraldehyde in 300 mL of dry dioxane was added 300 mg of hydroquinone (0.0027 mmol) and 60.0 g (1.13 mmol; 1.26 eq; 48.4 mL) of acrylonitrile. To this stirred solution was added all at once a freshly prepared solution of 3 g of NaOH dissolved in 60 mL of water and the whole was heated at 65° C. during 150 min. After cooling to 20° C., removal of the solvents under aspirator vacuum gave a residue which was partitioned between water and CH2Cl2. After separation, the aqueous layer was extracted 3 times with CH2Cl2 and the combined organic layers dried over Na2SO4 and concentrated under vacuum (aspirator). The crude residue was distilled under vacuum 81° C./lmm Hg) to yield 54 g (49%) of 4,4-dimethyl-5-oxovaleronitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04841045
Source datasetuspto-grants-1989_06
ORD IDord-02ef0ce0bcf74f7cac08b6310ab9ccdf
Source noteuspto-grants-1989_06