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Diisobutylaluminum hydride → 2-(3-Chloro-phenyl)-propane-1,2-diamine

HRID 1092360
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1092360
[NH2:1][C:2]([C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([Cl:12])[CH:7]=1)([CH3:5])[C:3]#[N:4].CC(C[AlH]CC(C)C)C>C1(C)C=CC=CC=1>[Cl:12][C:8]1[CH:7]=[C:6]([C:2]([NH2:1])([CH3:5])[CH2:3][NH2:4])[CH:11]=[CH:10][CH:9]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 14487Diisobutylaluminum hydrideHCID 167840712-Amino-2-(3-chloro-phenyl)-propionitrile

Produkt 1

HCID 574956392-(3-Chloro-phenyl)-propane-1,2-diamine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1140TolueneLösungsmittel2×

Versuchsvorschrift

A solution of compound 2-amino-2-(3-chloro-phenyl)-propionitrile (8.0 g) in toluene (60 mL) was cooled to −78° C. and DIBAL-H solution (132 mL of a 1M solution in toluene) was added to it drop wise under nitrogen. The reaction mixture was slowly warmed to room temperature and then left at stirring for 17 h. Reaction was monitored by TLC. After completion, the reaction mixture was quenched with 30 mL methanol and then 100 mL water. All solvents were evaporated and the crude mass was taken in 50 mL water and acidified to pH=1 with 1M HCl. Organic impurities were extracted with ethyl acetate and the aqueous layer was basified to pH=14 with 30% NaOH solution. The free diamine, 2-(3-chloro-phenyl)-propane-1,2-diamine, was extracted with dichloromethane, dried over sodium sulfate, filtered and concentrated (4.2 g). The material was used crude in the next reaction step. MS (ESI): 185.1 (MH+).

Aufarbeitung

  1. waitleft
  2. customReaction
  3. customAfter completion, the reaction mixture was quenched with 30 mL methanol
  4. customAll solvents were evaporated
  5. extractionOrganic impurities were extracted with ethyl acetate
  6. extractionThe free diamine, 2-(3-chloro-phenyl)-propane-1,2-diamine, was extracted with dichloromethane
  7. dry with materialdried over sodium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated (4.2 g)
  10. customin the next reaction step

Quellen und Nachweise

ORD-Eintrag
ord-8f6a41f9b6b34fe8bf2a3517a2e008d0
Quelldatensatz
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08129423B2

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