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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187021Generated: October 29, 2026

Sodium Chloride → N-(2,2-Dimethoxyethyl)-2-propenamide

https://huagongshe.com/reaction/2187021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantAcryloyl chlorideHCID 13140—
ReactantSodium HydroxideHCID 14798—
ReactantAminoacetaldehyde dimethyl acetalHCID 89728—
Catalyst2,2,6,6-tetramethyl-4-hydroxypiperidine-N-oxideHCID 11607999—
SolventWaterHCID 962—
ProductN-(2,2-Dimethoxyethyl)-2-propenamideHCID 989889981.7%

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-liter reactor having a stirrer and a cooling system. The sodium hydroxide solution is cooled to 10° C., and 105.1 g (1.0 mol) of aminoacetaldehyde dimethylacetal and 10 mg of the inhibitor 4-hydroxy-2,2,6,6-tetramethylpiperidin-1-oxide are added. 99.5 g (1.1 mol) of acrylic acid chloride are slowly added to that solution at 10° C. over a period of 2 hours. The pH value drops slowly and ultimately is adjusted to 7. According to GC, amine is no longer present. 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 concentrated using a rotary evaporator. The resulting oil is extracted three times with petroleum ether and then dried again using a rotary evaporator. 130 g of acrylamidoacetaldehyde dimethylacetal (81% of theory) are obtained in the form of an oil; the product is 99% according to GC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06407145B1
Source datasetuspto-grants-2002_06
ORD IDord-bf18d716daf442e4a2d29fa9bbcba490
Source noteuspto-grants-2002_06