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Hydrogen Sulfide → HCID 178478026, Verbindung

HRID 363745
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 363745
[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[C:4]#[N:5].C([N:12](CC)CC)C.S.[NH2:18][NH2:19].N([O-])=O.[Na+]>CO>[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[CH:6][C:3]=1[C:4]1[NH:5][N:12]=[N:19][N:18]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 5

HCID 402Hydrogen SulfideHCID 8471TriethylamineHCID 9321HydrazineHCID 133912-ChlorobenzonitrileHCID 23668193Sodium Nitrite

Produkt 1

HCID 178478026HCID 178478026, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887
Methanol
Lösungsmittel

Versuchsvorschrift

First, 35.6 mmol of 2-chlorobenzonitrile was dissolved in 50 ml of methanol, and 35.6 mmol of triethylarnine and 105 mmol of hydrogen sulfide were added thereto at room temperature, followed by adding 180 mmol of anhydrous hydrazine and keeping at the reflux temperature for 48 hours. The reaction mixture was evaporated under reduced pressure. The residue was dissolved in 50 ml of 5% hydrochloric acid, and 75 mmol of sodium nitrite was added thereto at 0° C. to cause reaction. After completion of the reaction, the reaction mixture was extracted with ethyl acetate to give 5-(2-chlorophenyl)tetrazole. Yield, 54%

Aufarbeitung

  1. customat room temperature
  2. customThe reaction mixture was evaporated under reduced pressure
  3. dissolutionThe residue was dissolved in 50 ml of 5% hydrochloric acid
  4. customat 0° C.
  5. customreaction
  6. customAfter completion of the reaction
  7. extractionthe reaction mixture was extracted with ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-27853476a6b94f57a0de9886991d656d
Quelldatensatz
uspto-grants-1999_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05874593

Notizen zur Reaktion

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