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Benzene → N-allyl-N-(1,3-dioxolan-2-ylmethyl)-alpha-chloroacetamide

HRID 1763775
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1763775
[CH2:1]([NH:4][CH2:5][CH:6]1[O:10][CH2:9][CH2:8][O:7]1)[CH:2]=[CH2:3].C1C=CC=CC=1.C(=O)([O-])[O-].[Na+].[Na+].[Cl:23][CH2:24][C:25](Cl)=[O:26]>O>[CH2:1]([N:4]([CH2:5][CH:6]1[O:10][CH2:9][CH2:8][O:7]1)[C:25](=[O:26])[CH2:24][Cl:23])[CH:2]=[CH2:3]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 241BenzeneHCID 6577Chloroacetyl chlorideHCID 10340Sodium CarbonateHCID 20441169N-Allyl-N-(1,3-dioxolan-2-ylmethyl)amine

Produkt 1

HCID 20307411N-allyl-N-(1,3-dioxolan-2-ylmethyl)-alpha-chloroacetamide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962
Water
Lösungsmittel

Versuchsvorschrift

N-Allyl-N-(1,3-dioxolan-2-ylmethyl)amine (9.2 grams), benzene (100 ml), water (100 ml) and sodium carbonate (8 grams) were charged into a glass reaction vessel equipped with a mechanical stirrer and reflux condenser. The mixture was cooled to about 5° to 10° C. and chloroacetyl chloride (5 ml) was added dropwise with stirring. After the addition was completed stirring was continued until the reaction mixture reached room temperature. After this time the organic phase was separated from the aqueous phase and was washed with water. The washed solution was then dried over anhydrous magnesium sulfate, filtered and stripped of solvent under reduced pressure to yield the desired product N-allyl-N-(1,3-dioxolan-2-ylmethyl)-α-chloroacetamide as an oil.

Aufarbeitung

  1. customequipped with a mechanical stirrer
  2. temperaturereflux condenser
  3. temperatureThe mixture was cooled to about 5° to 10° C.
  4. additionAfter the addition
  5. stirringwas completed stirring
  6. customreached room temperature
  7. customAfter this time the organic phase was separated from the aqueous phase
  8. washwas washed with water
  9. dry with materialThe washed solution was then dried over anhydrous magnesium sulfate
  10. filtrationfiltered

Quellen und Nachweise

ORD-Eintrag
ord-3be2eb94fd964e2daf9445add085e05a
Quelldatensatz
uspto-grants-1978_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04113464

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