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Hydrochloric Acid → 2-[5-(Benzylsulfanyl)-1H-tetrazol-1-yl]ethan-1-ol

HRID 1284633
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Reaktionsgleichung

Reaktionsgleichung von HRID 1284633
OCC[NH:4]C(=S)NN.C(Cl)C1C=CC=CC=1.[OH:17][CH2:18][CH2:19][N:20]=[C:21]([S:24][CH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)[NH:22][NH2:23].N([O-])=O.[Na+].Cl.C(=O)([O-])[O-].[K+].[K+]>O.CO>[OH:17][CH2:18][CH2:19][N:20]1[C:21]([S:24][CH2:25][C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)=[N:22][N:23]=[N:4]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

9

Edukt 6

HCID 313Hydrochloric AcidHCID 7503Benzyl ChlorideHCID 11430Potassium CarbonateHCID 20252217N-(2-Hydroxyethyl)hydrazinecarbothioamideHCID 23668193Sodium NitriteHCID 54026318HCID 54026318, Verbindung

Produkt 1

HCID 20252209
2-[5-(Benzylsulfanyl)-1H-tetrazol-1-yl]ethan-1-ol

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 887MethanolLösungsmittelHCID 962WaterLösungsmittel2×

Versuchsvorschrift

A mixture of 4-(2-hydroxyethyl)thiosemicarbazide (10.3 g), benzyl chloride (10.6 g), water (30 ml) and methanol (60 ml) was stirred for 20 hours at room temperature to give a homogeneous solution containing benzyl N-(2-hydroxyethyl)thiocarbazimidate. The solution was ice-cooled and thereto was little by little added sodium nitrite (5.24 g) with stirring and then dropwise added conc. hydrochloric acid (3.5 ml) over a period of 30 mimetes. The resulting mixture was stirred for an hour under ice-cooling. To the reaction mixture were added potassium carbonate (18 g) and water (30 ml). The mixture was stirred and then concentrated under reduced pressure. The concentrate was extracted with chloroform and the extract was washed with water, dried over magnesium sulfate and then evaporated under reduced pressure. The residual oil was subjected to column chromatography on silica gel. The fractions containing the object compound were collected to give an oil of 1-(2-hydroxyethyl)-5-benzylthio-1H-tetrazole (12.1 g).

Aufarbeitung

  1. customto give a homogeneous solution
  2. temperaturecooled
  3. stirringwith stirring
  4. stirringThe resulting mixture was stirred for an hour under ice-
  5. temperaturecooling
  6. stirringThe mixture was stirred
  7. concentrationconcentrated under reduced pressure
  8. extractionThe concentrate was extracted with chloroform
  9. washthe extract was washed with water
  10. dry with materialdried over magnesium sulfate
  11. customevaporated under reduced pressure
  12. additionThe fractions containing the object compound
  13. customwere collected

Quellen und Nachweise

ORD-Eintrag
ord-f3bfbe777e8c4ccbb086a8c94e6fb708
Quelldatensatz
uspto-grants-1986_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04563524

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