Citric Acid → 3-(aminomethyl)benzoic acid

HRID 376787Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 376787
Cl.CCN([CH:8]([CH3:10])[CH3:9])C(C)C.[NH:11](C(OC(C)(C)C)=O)[C@H](C(ON1C(=O)CCC1=O)=O)CC(=O)OCC1C=CC=CC=1.[C:41](O)(=O)[CH2:42][C:43]([CH2:48][C:49]([OH:51])=[O:50])(C(O)=O)O>CN(C=O)C.[Au]>[NH2:11][CH2:41][C:42]1[CH:43]=[C:48]([CH:10]=[CH:8][CH:9]=1)[C:49]([OH:51])=[O:50]

Komponenten

7

Edukt 4

HCID 311Citric AcidHCID 313Hydrochloric AcidHCID 81531DiisopropylethylamineHCID 135177984-Benzyl 1-(2,5-dioxopyrrolidin-1-yl) N-(tert-butoxycarbonyl)-L-aspartate

Produkt 1

HCID 5060733-(aminomethyl)benzoic acidAusbeute 92 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23985GoldKatalysatorHCID 6228DimethylformamideLösungsmittel2×

Reaktionsbedingungen

Temperatur
5 °C

Versuchsvorschrift

circle-solid.HCl (Mamb; 13.08 g, 70.0 mmol) was dissolved in 120 ml DMF and DIEA (24.32 ml, 140 mmol) was added, changing the pH from 4 to 7.5. The white suspension was stirred for 30 min at room temperature before a solution of Boc-Asp(OBzl)-OSu (29.40 g, 70.0 mmol) in DMF (50 ml) was added. The mixture was allowed to stir 24 hr, during which time it turned to a gold solution. The solution was added to 5% citric acid (2000 ml) and cooled to 5° C. for 3 hr. The solids were then collected by filtration, washed with ice cold water (200 ml) and ice cold ethyl ether (100 ml), and dried under reduced pressure to give the title compound as a colorless solid (29.62 g, 92%); MP=149-151° C.; DCI-MS: [M+NH4 ]=474.

Aufarbeitung

  1. additionwas added
  2. filtrationThe solids were then collected by filtration
  3. washwashed with ice cold water (200 ml) and ice cold ethyl ether (100 ml)
  4. customdried under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-22250e18af714492982e35ec314fc18a
Quelldatensatz
uspto-grants-2000_02
Patentnummer
US06022523

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