HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2058869Generated: October 31, 2026
Dimethylformamide dimethyl acetal → HCID 20548490, compound
https://huagongshe.com/reaction/2058869
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Reactant | HCID 20548491 | HCID 20548491 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 20548490 | HCID 20548490 | — |
Reaction Steps
To a 6 g. portion of crude 1-(3-trifluoromethylphenyl)-2,4-octanedione was added 40 ml. of N,N-dimethylformamide dimethyl acetal and a few milliliters of methanol. The mixture was stirred under reflux overnight, and was then evaporated under vacuum to obtain 8.9 g. of a thick dark oil. The oil was taken up in 50 ml. of methanol, 9 g. of methylamine hydrochloride was added, and the mixture was stirred under reflux for 3 hours. It was then evaporated to a semi-solid under vacuum, and the residue was partitioned between diethyl ether and water. The organic layer was dried over magnesium sulfate and evaporated under vacuum. The residue was chromatographed on a 300 g. silica gel column with 2:3 ethyl acetate:dichloromethane, and the product-containing fractions were combined and evaporated under vacuum to obtain 0.17 g. of the desired product in impure form. Nmr analysis in DMSOd6 showed peaks at δ7.6-8.3 (m, 6H, aromatic); 3.8 (s, 3H, N--CH3); 3.0-3.3 (t, 2H, COCH2); 0.7-1.8 (m, 7H, CH2CH2CH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04319916 |
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| Source dataset | uspto-grants-1982_03 |
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| ORD ID | ord-05783392b09f4819beb4690f9cc1aba2 |
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| Source note | uspto-grants-1982_03 |
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