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L-Aspartic Acid → Aspartic acid, potassium salt

HRID 1598350
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1598350
[NH2:1][C@H:2]([C:7]([OH:9])=[O:8])[CH2:3][C:4]([OH:6])=[O:5].[OH-].[K+:11]>O>[NH2:1][C@H:2]([C:7]([O-:9])=[O:8])[CH2:3][C:4]([O-:6])=[O:5].[K+:11].[K+:11]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 5960L-Aspartic Acid2×HCID 14797Potassium Hydroxide

Produkt 1

HCID 6454950Aspartic acid, potassium salt

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Reaktionsbedingungen

Temperatur
70 °C

Versuchsvorschrift

To a 500 ml 2-neck round bottom flask, equipped with a reflux condenser and a pressure equalizing addition funnel was charged 10.00 parts (0.068 eqv.) of aspartic acid. 101 ml of KOH (0.065 eqv.) was added to the addition funnel. The basic solution was added to the aspartic acid, with magnetic stirring, over about 4 minutes. The reaction mixture was then stirred at about 70° C. for an additional hour, to insure complete reaction. The water was stripped off the reaction product at about 10 mm Hg and about 70° C. The white powder was broken up and dried overnight at about 80° C. and at about 2 mm Hg. A freely flowing powder was obtained and stored in a dry, airtight container.

Aufarbeitung

  1. customTo a 500 ml 2-neck round bottom flask, equipped with a reflux condenser
  2. additionaddition funnel
  3. customreaction
  4. customat about 10 mm Hg and about 70° C
  5. customdried overnight at about 80° C. and at about 2 mm Hg
  6. customwas obtained

Quellen und Nachweise

ORD-Eintrag
ord-451db8127fff4036a65b4e9635217885
Quelldatensatz
uspto-grants-1998_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05736587

Notizen zur Reaktion

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