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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286731Generated: November 2, 2026

5-Oxo-5-phenylvaleronitrile → 5-Hydroxy-5-phenylvaleronitrile

https://huagongshe.com/reaction/2286731

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Oxo-5-phenylvaleronitrileHCID 312663—
ReactantLithium borohydrideHCID 4148881—
Product5-Hydroxy-5-phenylvaleronitrileHCID 14172270—

Reaction Steps

A mixture of 41 g. (0.25 mole) of 5-hydroxy-5-phenylvaleronitrile, obtained from 4-benzoylbutyronitrile by lithium borohydride reduction by the procedure of Colonge et. al., Bull. Soc. Chem. France, 2005-2011 (1966); Chem. Abstr., 65, 18547d (1966), and 0.30 mole of potassium hydroxide in 200 ml. of water was heated at reflux for eight hours. The mixture was cooled to room temperature and neutralized with 10 M hydrochloric acid, saturated with sodium chloride and extracted with ether several times. The extracts were washed with water, dried (Na2SO4) and the ether evaporated to obtain dl-5-phenyl-5-hydroxyvaleric acid lactone which was recrystallized from dilute alcohol, M.P. 62.5° C., 79% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04267331
Source datasetuspto-grants-1981_05
ORD IDord-93d40534b0ac4f1bacaea67139499e0f
Source noteuspto-grants-1981_05