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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267484Generated: October 29, 2026

Sulfuric Acid → N-(1,1-dimethyl-3-dimethylaminopropyl)acrylamide

https://huagongshe.com/reaction/267484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantAcrylonitrileHCID 7855—
ReactantSodium HydroxideHCID 14798—
Reactant2,6-Di-tert-butyl-4-methylphenolHCID 31404—
Reactant2-Buten-1-amine, N,N,3-trimethyl-HCID 5259975—
SolventWaterHCID 962—
ProductN-(1,1-dimethyl-3-dimethylaminopropyl)acrylamideHCID 1639462—

Reaction Conditions

Temperature0 °C

Reaction Steps

A resin flask is cooled to 0° C. and 450 grams (8.5 moles) of acrylonitrile, 1020 grams (10 moles) of sulfuric acid and 37 grams of water are added. To this mixture are then added 475 grams (4.2 moles) of the 1-dimethylamino-3-methyl-2-butene prepared as described above, and 8.5 grams of 2,6-di-t-butyl-p-cresol. The mixture is stirred at 68° C. for about 1 hour and is then neutralized with about 30% sodium hydroxide. The organic layer is separated, diluted with 2050 ml. of methanol and neutralized with ammonia. An additional 1000 ml. of methanol is added and the solution is filtered. The methanol is stripped from the filtrate and the residue is distilled. There is obtained 400 grams (64.5% of the theoretical amount) of the desired N-(1,1-dimethyl-3-dimethylaminopropyl)acrylamide boiling at 75°-92° C./0.25-0.9 mm. The nitrogen analysis is 15.4%, as compared with a theoretical value of 15.2%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03943114
Source datasetuspto-grants-1976_03
ORD IDord-e12ee3a14c334806b57a51ab2aee0df8
Source noteuspto-grants-1976_03