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

HRID 364676

Reaktionsgleichung

Reaktionsgleichung von HRID 364676
[CH2:1]([CH:3]([CH2:6][CH2:7][CH2:8][CH3:9])[CH2:4][NH2:5])[CH3:2].[C:10]([CH:14]1CC2O[CH:15]1C=C2)(OC)=[O:11].Cl.C(Cl)Cl>O>[CH2:1]([CH:3]([CH2:6][CH2:7][CH2:8][CH3:9])[CH2:4][NH:5][C:10](=[O:11])[CH:14]=[CH2:15])[CH3:2]

Komponenten

6

Reaktionsbedingungen

Temperatur
140 °C

Versuchsvorschrift

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.

Aufarbeitung

  1. temperatureduring cooling
  2. customthe organic phase separated off
  3. extractionthe aqueous phase extracted twice with 25 ml methylene chloride in each instance
  4. customThe combined organic phases are reduced in a rotary evaporator at a bath temperature of 90° C.
  5. customOn conclusion of the furane separation
  6. temperaturethe sedimentation temperature increases
  7. distillationthe product distills over

Quellen und Nachweise

ORD-Eintrag
ord-40c98682a7514ca69888367bd7e5dca6
Quelldatensatz
uspto-grants-1986_08
Patentnummer
US04605740

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