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Water → (S)-3-(2-Nitro-phenylamino)-hexanoic acid ethyl ester

HRID 1747373
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1747373
F[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[N+:8]([O-:10])=[O:9].[CH2:11]([O:13][C:14](=[O:21])[CH2:15][C@@H:16]([NH2:20])[CH2:17][CH2:18][CH3:19])[CH3:12].C(N(C(C)C)CC)(C)C.O>CN(C=O)C>[CH2:11]([O:13][C:14](=[O:21])[CH2:15][C@@H:16]([NH:20][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[N+:8]([O-:10])=[O:9])[CH2:17][CH2:18][CH3:19])[CH3:12]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 962WaterHCID 738951-Fluoro-2-nitrobenzeneHCID 81531DiisopropylethylamineHCID 10773249Ethyl (3S)-3-aminohexanoate

Produkt 1

HCID 59497566(S)-3-(2-Nitro-phenylamino)-hexanoic acid ethyl esterAusbeute 81 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228
Dimethylformamide
Lösungsmittel

Versuchsvorschrift

To a solution of 1-fluoro-2-nitrobenzene (500 mg, 3.5 mmol) in DMF (150 mL) were added (S)-3-Amino-hexanoic acid ethyl ester (600 mg, 3.8 mmol) and diisopropyl ethylamine (0.65 mL, 3.8 mmol). The solution was heated to 90 C for 16 hours. The solution was cooled down and was water (300 mL) was added. The solution was extracted with EtOAc and the combined organic layer was dried with MgSO4. The mixture was filtered and the filtrate was concentrated. The residue was purified by CombiFlash with 5% EtOAc in Hexane as the eluent to afford the desirable product (S)-3-(2-Nitro-phenylamino)-hexanoic acid ethyl ester (795 mg, 80%) as a colorless oil.

Aufarbeitung

  1. temperatureThe solution was heated to 90 C for 16 hours
  2. temperatureThe solution was cooled down
  3. additionwas added
  4. extractionThe solution was extracted with EtOAc
  5. dry with materialthe combined organic layer was dried with MgSO4
  6. filtrationThe mixture was filtered
  7. concentrationthe filtrate was concentrated
  8. customThe residue was purified by CombiFlash with 5% EtOAc in Hexane as the eluent

Quellen und Nachweise

ORD-Eintrag
ord-077cb6fd19544d829273c2e7739df948
Quelldatensatz
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09150556B2

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