HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 839180Generated: October 26, 2026
Acetic Acid → N-(1,1-Dimethyl-3-oxobutyl)-2-diethylphosphonoacrylamide
https://huagongshe.com/reaction/839180
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Diethyl (3-oxobutyl)phosphonate | HCID 14033 | — |
| Reactant | Diethylphosphite | HCID 3780918 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 4-Acrylamido-4-methyl-2-pentanone | HCID 21584921 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(1,1-Dimethyl-3-oxobutyl)-2-diethylphosphonoacrylamide | HCID 21328247 | 97% |
Reaction Steps
Using the same procedure of Example 1 for the preparation of diethyl 3-oxobutylphosphonate, a solution prepared from the reaction of 3.1 grams (0.135 mole) of sodium with 63 ml of anhydrous ethanol was added under nitrogen and drying conditions with stirring at room temperature to 152 grams (1 mole) of diethyl phosphite. To this solution was then added over a one hour period maintaining the internal temperature at 30°-40° C with external cooling, 169 grams (1 mole) of diacetone acrylamide. The solution was then stirred for another hour at 24° C before 8.2 grams (0.135 mole) of acetic acid was slowly added to bring the pH to 5. The solution was dried at 70° C/16 mm and topped off by distillation for 30 minutes with a maximum pot temperature of 120° C at 0.2 mm. The pot residue (316 grams) was the desired N-(1,1-dimethyl-3-oxybutyl)-2-diethylphosphonoacrylamide in a 97% yield. Structure of the desired product with a purity of about 95% was confirmed by NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04093809 |
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| Source dataset | uspto-grants-1978_06 |
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| ORD ID | ord-a5484eff53fa4fff8a8bf3ecfe62954b |
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| Source note | uspto-grants-1978_06 |
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