HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359571Generated: October 29, 2026
Dimethylformamide → 4-[Bis[2-(acetyloxy)ethyl]amino]benzaldehyde
https://huagongshe.com/reaction/359571
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ethanol, 2,2'-(phenylimino)bis-, 1,1'-diacetate | HCID 29521 | — |
| Reactant | Sodium Acetate Trihydrate | HCID 23665404 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-[Bis[2-(acetyloxy)ethyl]amino]benzaldehyde | HCID 328729 | — |
Reaction Steps
To 450 ml of dry dimethyl formamide were slowly added dropwise with stirring and at a temperature of 0°-10° C. 100 ml of freshly distilled phosphoroxytrichloride. This mixture was stirred for 2 hours at 20° C. To this mixture there was subsequently added dropwise with proper stirring and over a period of 60 minutes the crude reaction product of the previous step, viz. N,N-di(2-acetyloxyethyl)aniline, the reaction mixture being kept at a temperature of 20° C. Next, the reaction mixture was heated to 60° C. for 60 minutes and then poured, with vigorous stirring, into a mixture of 1 kg of ice and a solution of 525 g of sodium acetate trihydrate in 1 l of water. The organic layer was separated and the water layer was extracted four times, each time with 300 ml of dichloromethane. The combined organic layers were washed three times, each time with 200 ml of water, dried on magnesium sulphate, and concentrated by evaporation. The residue (about 280 g of dark brown oil), which consisted almost entirely of 4-di(2-acetyloxyethyl)aminobenzaldehyde, was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05001209 |
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| Source dataset | uspto-grants-1991_03 |
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| ORD ID | ord-2ca2f2b4414a493a89fdc5b5e73d9298 |
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| Source note | uspto-grants-1991_03 |
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