ethyl N-(2,3-dichloro-6-nitrobenzyl)glycine hydrochloride → ethyl-N-(6-amino-2,3-dichlorobenzyl)glycine

HRID 481142

Reaktionsgleichung

Reaktionsgleichung von HRID 481142
Cl.[CH2:2]([N:4]([CH2:9][C:10]1[C:15]([N+:16]([O-])=O)=[CH:14][CH:13]=[C:12]([Cl:19])[C:11]=1[Cl:20])[CH2:5][C:6]([OH:8])=[O:7])[CH3:3]>O.C(O)C.[Pt]>[CH2:2]([N:4]([CH2:9][C:10]1[C:15]([NH2:16])=[CH:14][CH:13]=[C:12]([Cl:19])[C:11]=1[Cl:20])[CH2:5][C:6]([OH:8])=[O:7])[CH3:3]

Komponenten

5

Edukt 1

HCID 66640009ethyl N-(2,3-dichloro-6-nitrobenzyl)glycine hydrochloride2×

Produkt 1

HCID 67080112ethyl-N-(6-amino-2,3-dichlorobenzyl)glycineAusbeute 72 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 23939PlatinumKatalysatorHCID 702EthanolLösungsmittelHCID 962WaterLösungsmittel

Versuchsvorschrift

A solution of 0.344 g of ethyl N-(2,3-dichloro-6-nitrobenzyl)glycine hydrochloride (compound VI) in 1.5 mL of water and 1.5 mL ethanol (with 5% isopropanol) was stirred and 5% sulfided platinum on carbon under hydrogen (50 to 100 psi) for 16 hours. The catalyst was removed by filtration. The filtrate concentrated, diluted with water and toluene, and basified (aqueous sodium hydroxide or potassium carbonate) to pH 9-10. The organic phase was separated, concentrated, and the crude material purified by low-temperature recrystallization from toluene in hexane to give compound I in 72% yield.

Aufarbeitung

  1. customThe catalyst was removed by filtration
  2. concentrationThe filtrate concentrated
  3. additiondiluted with water and toluene, and basified (aqueous sodium hydroxide or potassium carbonate) to pH 9-10
  4. customThe organic phase was separated
  5. concentrationconcentrated
  6. customthe crude material purified by low-temperature recrystallization from toluene in hexane

Quellen und Nachweise

ORD-Eintrag
ord-5ecaf55e573e49b5b990f95c786a5cfc
Quelldatensatz
uspto-grants-2003_11
Patentnummer
US06653500B2

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