HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 621645Generated: October 30, 2026
Ethyl formate → 2-Formyl-2-phenylacetonitrile
https://huagongshe.com/reaction/621645
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | Phenylacetonitrile | HCID 8794 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-Formyl-2-phenylacetonitrile | HCID 345880 | — |
Reaction Steps
To a suspension of sodium methoxide (5.56 g) in benzene (200 ml) is added dropwise with stirring a mixture of ethyl formate (8.14 g) and phenylacetonitrile (11.7 g) under ice cooling. After 30 minutes, the ice bath is taken off. After reacting for 3 hours, ice water is added to the reaction mixture, and the aqueous layer is separated. The organic layer is washed with 0.5 N sodium hydroxide solution (50 ml×3), and the aqueous layer and the washings are combined and adjusted to pH 3-4 with conc. hydrochloric acid. The mixture is stirred under ice cooling for 20 minutes, and the resulting precipitate is separated by filtration and washed with water to give α-formylphenylacetonitrile. The product is used in the subsequent procedure without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04824834 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-a2c44c8e1ee345e0af81bb0a05d792ff |
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| Source note | uspto-grants-1989_04 |
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