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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 3-Phenoxybenzaldehyde | HCID 38284 | — |
| Reactant | Bisulfite | HCID 104748 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzeneacetonitrile, alpha-hydroxy-3-phenoxy-, (alphaS)- | HCID 93218 | 1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04202835 |
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| Source dataset | uspto-grants-1980_05 |
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| ORD ID | ord-1cf01f86b10a41628f99d739cd81becd |
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| Source note | uspto-grants-1980_05 |
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