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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2037397Generated: October 30, 2026

Acetonitrile → 3-Hydroxy-3-phenylbutanenitrile

https://huagongshe.com/reaction/2037397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantAcetophenoneHCID 7410—
ReactantAmmonium ChlorideHCID 25517—
SolventTetrahydrofuranHCID 8028—
Product3-Hydroxy-3-phenylbutanenitrileHCID 53923375%

Reaction Conditions

Temperature-20 °C

Reaction Steps

Dry THF was cooled to −20° C. and 2.5 M n-Bull (100 mL, 0.25 mol) was added. A solution of CH3CN (11.25 g, 0.25 mol) in dry THF was added dropwise over 10 min. Then the mixture was stirred for 1 h at −20° C. and a solution of acetophenone (30 g, 0.25 mol) in THF was added dropwise over 10 min. The mixture was stirred at −20° C. for 15 min and warmed to rt over 15 min. Aq NH4Cl was added to quench the reaction. The solution was extract with EtOAc. The organic layer washed with brine, dried over anhydrous Na2SO4 and concentrated to give 3-hydroxy-3-phenylbutanenitrile (30 g, yield 75%). 1H NMR (CDCl3, 400 MHZ): δ=1.76 (s, 3H), 2.83 (s, 2H), 7.34 (m, 1H), 7.41 (m, 2H), 7.5 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575156B2
Source datasetuspto-grants-2013_11
ORD IDord-098613622b004fab9581a9912188d006
Source noteuspto-grants-2013_11