HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351307Generated: November 2, 2026
Methanol → alpha-(3,4-Dimethoxy-benzal)-beta-methoxy-propionitrile
https://huagongshe.com/reaction/2351307
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Veratraldehyde | HCID 8419 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Propanenitrile, 3-methoxy- | HCID 61032 | — |
| Solvent | Water | HCID 962 | — |
| Product | alpha-(3,4-Dimethoxy-benzal)-beta-methoxy-propionitrile | HCID 111305 | 100% |
Reaction Steps
A mixture of 200 g (1.20 mole) of 3,4-dimethoxy-benzaldehyde, 150 g (1.75 mole) of β-methoxy-propinitrile, 260 ml of methanol and 10 g of a 55% methanolic potassium hydroxide solution is stirred at 60°-62° C. for 8 hours, whereupon the reaction mixture is cooled to 30° C., and 170 g of a 55% methanolic potassium hydroxide solution are added dropwise. The reaction mixture is stirred for 5 hours and diluted with 1000 ml of water. The precipitated crystalline product is filtered, washed with methanol and water. Thus 280 g of α-(3,4-dimethoxy-benzal)-β-methoxy-propionitrile are obtained, yield 85%, mp.: 82°-83° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04873249 |
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| Source dataset | uspto-grants-1989_10 |
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| ORD ID | ord-ef0842d94a3849718e1bcac0753f13a2 |
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| Source note | uspto-grants-1989_10 |
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