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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395124Generated: October 30, 2026

Ethyl Acetate → Benzeneacetonitrile, alpha-hydroxy-3-phenoxy-, (alphaS)-

https://huagongshe.com/reaction/1395124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium CyanideHCID 8929—
Reactant3-PhenoxybenzaldehydeHCID 38284—
ReactantBisulfiteHCID 104748—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductBenzeneacetonitrile, alpha-hydroxy-3-phenoxy-, (alphaS)-HCID 932181%

Reaction Conditions

Temperature10 °C

Reaction Steps

A solution of 0.765 Kg of sodium cyanide in 3.8 liters of water was added with stirring at 5° C. over 10 minutes to a mixture of 3.700 Kg of combination bisulfite of m-phenoxy-benzaldehyde (98% titer) in 7.4 liters of dimethylformamide and 3.8 liters of acetic acid were added thereto over 30 minutes at 5° C. The mixture was stirred for 30 minutes at 10° C. and the reaction mixture was then poured into a mixture of water and ethyl acetate. The mixture was stirred and decanted and the aqueous phase was extracted twice more with ethyl acetate. The combined ethyl acetate phases were washed with water, dried and stirred with 0.37 Kg of activated charcoal and 0.37 Kg of sodium sulfate. The mixture was filtered and the filtrate was evaporated to dryness under reduced pressure to obtain 2.770 Kg of α-cyano-3-phenoxy-benzyl alcohol containing 1% of dimethylformamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04202835
Source datasetuspto-grants-1980_05
ORD IDord-1cf01f86b10a41628f99d739cd81becd
Source noteuspto-grants-1980_05