Trichloromethanethiol → 3-Benzyl-5-chloro-1,2,4-thiadiazole

HRID 2063668

Reaktionsgleichung

Reaktionsgleichung von HRID 2063668
Cl.[C:2]1([CH2:8][C:9]([NH2:11])=[NH:10])[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Cl:12][C:13]([SH:16])(Cl)Cl.[OH-].[Na+]>ClCCl.O>[CH2:8]([C:9]1[N:11]=[C:13]([Cl:12])[S:16][N:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Komponenten

6

Reaktionsbedingungen

Temperatur
-10 °C

Versuchsvorschrift

To a suspension of 2-phenyl-acetamidine hydrochloride (1.078 g, 6 mmol) in dichloromethane (10 ml) was added perchloromethyl mercaptan (0.61 ml, 5 mmol) via syringe. The mixture was cooled in an ice-methanol bath to −10° C. and a solution of sodium hydroxide (1.2 g, 30 mmol) in water (3 ml) was added dropwise keeping the temperature below −8° C. After complete addition the mixture was stirred 10 min at 0° C. The reaction mixture was diluted with water and the aqueous phase was extracted three times with dichloromethane. The combined organic phases were dried over Na2SO4, filtered and the solvents were evaporated. The residue was purified by chromatography on silica gel using heptane/ethyl acetate as eluent. The title compound was obtained as an orange liquid (0.779 g, 62%). MS ISP (m/e): 211.0 (100) [(M+H)+].

Aufarbeitung

  1. customthe temperature below −8° C
  2. additionAfter complete addition the mixture
  3. extractionthe aqueous phase was extracted three times with dichloromethane
  4. dry with materialThe combined organic phases were dried over Na2SO4
  5. filtrationfiltered
  6. customthe solvents were evaporated
  7. customThe residue was purified by chromatography on silica gel

Quellen und Nachweise

ORD-Eintrag
ord-6a1148a8413e4bdcaaa3569775836b6b
Quelldatensatz
uspto-grants-2012_10
Patentnummer
US08288403B2

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