2-Chlorocyclopentanone → 3,4,5,6-Tetrahydro-2H-cyclopenta(d)(1,3)thiazol-2-imine

HRID 589174

Reaktionsgleichung

Reaktionsgleichung von HRID 589174
Cl[CH:2]1[CH2:6][CH2:5][CH2:4][C:3]1=O.[NH2:8][C:9]([NH2:11])=[S:10]>O1CCOCC1>[S:10]1[C:3]2[CH2:4][CH2:5][CH2:6][C:2]=2[N:8]=[C:9]1[NH2:11]

Komponenten

4

Versuchsvorschrift

2-Chlorocyclopentanone (9.01 g, 74.4 mmol) was added slowly to a 95° C. stirred mixture of thiourea (5.77 g, 75.0 mmol) in 1,4-dioxane (150 mL). After full addition, the temperature was maintained for an hour then the mixture was cooled to room temperature. It was then filtered and washed with 1,4-dioxane and diethyl ether, and dried under air suction to afford 11.15 g white solid. This was partitioned between diethyl ether and saturated aqueous sodium carbonate. The ether layer was washed with brine, dried with Na2SO4, and solvent removed by rotoevaporation to afford 9.8 g beige solid. (Modified procedure from US Patent application 64 699, 2008, Florjancic, A. S.; et al).

Aufarbeitung

  1. additionAfter full addition
  2. temperaturethe temperature was maintained for an hour
  3. filtrationIt was then filtered
  4. washwashed with 1,4-dioxane and diethyl ether
  5. customdried under air suction

Quellen und Nachweise

ORD-Eintrag
ord-1928173ea33e40c88666c8de3bd978bb
Quelldatensatz
uspto-grants-2016_01
Patentnummer
US09227971B2

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