HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584510Generated: October 25, 2026
Sodium Chloride → N-(2,2-Dimethoxyethyl)-2-propenamide
https://huagongshe.com/reaction/1584510
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aminoacetaldehyde dimethyl acetal | HCID 89728 | — |
| Catalyst | 2,2,6,6-tetramethyl-4-hydroxypiperidine-N-oxide | HCID 11607999 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(2,2-Dimethoxyethyl)-2-propenamide | HCID 9898899 | 81.7% |
Reaction Steps
40 g (1.0 mol) of sodium hydroxide are dissolved in 100 g of water and 200 g of ice in a 1 litre reactor fitted with stirring and cooling means. The sodium hydroxide solution is cooled to 10° C., and 105.1 g (1.0 mol) of aminoacetaldehyde dimethyl acetal and 10 mg of the inhibitor 4-hydroxy-2,2,6,6-tetrarnethylpiperidine 1-oxide are added. 99.5 g (1.1 mol) of acryloyl chloride are slowly added to this solution at 10° C. over the course of 2 hours. The pH drops slowly and is finally set to pH=7. Amine is no longer present according to GC. The reaction mixture is saturated with sodium chloride and extracted three times with 200 ml of tert-butyl methyl ether. The organic phase is dried, filtered and evaporated on a rotary evaporator. The resultant oil is extracted three times with petroleum ether and subsequently re-dried on a rotary evaporator, giving 130 g of acrylamidoacetaldehyde dimethyl acetal (81% of theory) as an oil. The product is 99% pure according to GC. ##STR29##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05932674 |
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| Source dataset | uspto-grants-1999_08 |
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| ORD ID | ord-9629e37cf3c240cc86c1b4dfe34b6af6 |
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| Source note | uspto-grants-1999_08 |
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