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Hydrochloric Acid → 3-(Aminomethyl)-2-chlorobenzonitrile

HRID 1051946
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1051946
Br[CH2:2][C:3]1[C:4]([Cl:11])=[C:5]([CH:8]=[CH:9][CH:10]=1)[C:6]#[N:7].[N-:12]=[N+]=[N-].[Na+].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.Cl>CN(C=O)C.CCOC(C)=O>[Cl:11][C:4]1[C:5]([C:6]#[N:7])=[CH:8][CH:9]=[CH:10][C:3]=1[CH2:2][NH2:12]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 313Hydrochloric AcidHCID 11776TriphenylphosphineHCID 33557Sodium AzideHCID 571606383-(Bromomethyl)-2-chlorobenzonitrile

Produkt 1

HCID 897048733-(Aminomethyl)-2-chlorobenzonitrile

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6228
Dimethylformamide
Lösungsmittel
HCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

To a soln. of 3-(bromomethyl)-2-chlorobenzonitrile (0.87 mmol) in 9 mL DMF was added NaN3 (1.3 mmol) and the resulting brown solution was stirred at RT for 20 min. The reaction mixture was diluted with EtOAc, washed twice with water and brine, dried over MgSO4 and concentrated in vacuo. The crude azide was redissolved in 4.3 mL THF and 0.1 mL water. Triphenylphosphine (1.04 mmol) was added and the mixture was stirred at RT overnight. The reaction mixture was acidified with 0.1; N HCl soln. until pH 3 and it was extracted 3 times with Et2O. The aq. phase was basified with 1M NaOH soln. and extracted 3 times with DCM. The comb. org. layers were dried over MgSO4 and conc. in vacuo to give the desired product as yellowish oil.

Aufarbeitung

  1. washwashed twice with water and brine
  2. dry with materialdried over MgSO4
  3. concentrationconcentrated in vacuo
  4. dissolutionThe crude azide was redissolved in 4.3 mL THF
  5. stirringthe mixture was stirred at RT overnight
  6. extractionuntil pH 3 and it was extracted 3 times with Et2O
  7. extractionand extracted 3 times with DCM
  8. dry with materiallayers were dried over MgSO4 and conc. in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-30b259af35c249f891632696c55c878c
Quelldatensatz
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09388197B2

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