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Glycine → Acryloylglycine

HRID 874052
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 874052
[NH2:1][CH2:2][C:3]([OH:5])=[O:4].[C:6](Cl)(=[O:9])[CH:7]=[CH2:8]>[OH-].[Na+]>[C:6]([NH:1][CH2:2][C:3]([OH:5])=[O:4])(=[O:9])[CH:7]=[CH2:8]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 750GlycineHCID 13140Acryloyl chloride

Produkt 1

HCID 100321AcryloylglycineAusbeute 32,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 14798Sodium HydroxideLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

7.5 g (0.1 mol) mol) glycine was dissolved in 100 ml 2 N NaOH. The solution was cooled to 0° C. and 10.8 g (0.12 mol) acryloyl chloride was added dropwise over 45 minutes, while the temperature was kept below 10° C. The reaction was allowed to continue for one hour at 10° C. The reaction mixture was extracted 2 times with 50 ml tert. butyl methyl ether. The pH was adjusted to pH=3, using a concentrated hydrochloric acid solution and the reaction mixture was saturated with sodium chloride. The mixture was extracted 5 times with 100 ml n.-pentanol. The pooled n.-pentanol fractions were dried over Na2SO4 and evaporated under reduced pressure, after addition of a small fraction BHT as stabilizer. 4.2 g (32.5%) of N-acryloyl-glycine was isolated (m.p. 124-126° C.). N-acryloyl-glycine is Comparative Monomer 5 (see below).

Aufarbeitung

  1. customwas kept below 10° C
  2. extractionThe reaction mixture was extracted 2 times with 50 ml tert. butyl methyl ether
  3. extractionThe mixture was extracted 5 times with 100 ml n
  4. dry with material-pentanol fractions were dried over Na2SO4
  5. customevaporated under reduced pressure
  6. additionafter addition of a small fraction BHT as stabilizer

Quellen und Nachweise

ORD-Eintrag
ord-944211383c444fa4b64675c3187bedf3
Quelldatensatz
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08978554B2

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