HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128163Generated: October 25, 2026
1,1-Dimethoxyethyl(dimethyl)amine → 2-(p-Fluorobenzoyl)-3-dimethylaminocrotononitrile
https://huagongshe.com/reaction/128163
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1-Dimethoxyethyl(dimethyl)amine | HCID 87835 | — |
| Reactant | p-Fluorobenzoylacetonitrile | HCID 2783172 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-(p-Fluorobenzoyl)-3-dimethylaminocrotononitrile | HCID 23468497 | — |
Reaction Steps
To a solution of 1.6 g. of p-fluorobenzoylacetonitrile [Pihl et al., Reakts. Sposobnost Org. Soedin. Tartu. Gos. Univ., 5 (1), 27, (1968)] in 30 ml. of chloroform, cooled to -10° C., is added 1.4 g. of N,N-dimethylacetamide dimethylacetal. The reaction mixture is stirred at -10° C. for 2 hours and then evaporated in vacuo to an oil. This oil is dissolved in 150 ml. of benzene and filtered through Magnesol®. The filtrate is evaporated to 50 ml. and petroleum ether is added to effect crystallization. The product is collected by filtration and then recrystallized from benzene-petroleum ether with charcoal treatment giving the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04259256 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-7c5808a82e174b9fa1fa2e1ca3f810ae |
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| Source note | uspto-grants-1981_03 |
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