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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 364676Erstellt: 26. Oktober 2026

Hydrochloric Acid → 2-Propenamide, N-(2-ethylhexyl)-

https://huagongshe.com/reaction/364676

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktDichloromethaneHCID 6344—
Edukt2-EthylhexylamineHCID 7719—
EduktMethyl 7-oxabicyclo[2.2.1]hept-5-ene-2-carboxylateHCID 12271748—
LösungsmittelWaterHCID 962—
Produkt2-Propenamide, N-(2-ethylhexyl)-HCID 10464979—

Reaktionsbedingungen

Temperatur140 °C

Reaktionsschritte

7.2 parts 30% methanolic Na-methylate solution are added to 64.5 parts 2-ethylhexylamine. 77 parts 2-carbomethoxy-7-oxabicyclo(2,2,1)hept-5-ene are added drop-wise at 30° to 35° C. during cooling. The reaction medium is then stirred for 15 hours and neutralised with 4 parts concentrated hydrochloric acid. 100 parts methylene chloride and 50 parts water are added, the organic phase separated off, and the aqueous phase extracted twice with 25 ml methylene chloride in each instance. The combined organic phases are reduced in a rotary evaporator at a bath temperature of 90° C. and a vacuum of 20 Torr. The residue is heated under a high vacuum to 110° to 120° C. (bath temperature 140° C.). On conclusion of the furane separation, the sedimentation temperature increases and the product distills over. 66.6 parts N(2-ethylhexyl)acrylamide with a boiling point of 123° C. at 0.4 Torr are obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04605740
Quelldatensatzuspto-grants-1986_08
ORD IDord-40c98682a7514ca69888367bd7e5dca6
Quellennotizuspto-grants-1986_08