Dodecylamine → 1-(3-Methoxybenzyl)-3-Dodecyl Thiourea

HRID 1375751

Reaktionsgleichung

Reaktionsgleichung von HRID 1375751
[CH2:1]([NH2:13])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].[CH3:14][O:15][C:16]1[CH:17]=[C:18]([CH:23]=[CH:24][CH:25]=1)[CH2:19][N:20]=[C:21]=[S:22]>C(O)C>[CH3:14][O:15][C:16]1[CH:17]=[C:18]([CH:23]=[CH:24][CH:25]=1)[CH2:19][NH:20][C:21]([NH:13][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12])=[S:22]

Komponenten

4

Edukt 2

HCID 13583DodecylamineHCID 1265123-Methoxybenzyl isothiocyanate

Produkt 1

HCID 101334051-(3-Methoxybenzyl)-3-Dodecyl Thiourea

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Reaktionsbedingungen

Temperatur
4 °C

Versuchsvorschrift

Dodecyl amine (4.89 g, 26.4 mmol) in 83 ml ethanol at 50° C. was reacted with 3-methoxybenzyl isothiocyanate (3.97 g, 22.1 mmol) for 6 h under N2 with stirring, and then poured into a 250 ml beaker. Performing this reaction at 40° C. led to a precipitate that was difficult to stir. Crystallization began as soon as the reaction started cooling below 50° C. The reaction mixture was cooled to 4° C. and the crystals were filtered off using Whatman 54 filter paper. The crystals were washed with 15 ml of ethanol. Combined filtrates were evaporated to dryness and taken up in 10 ml ethanol. Cooling the solution to −10° C. gave no crystals. The solution was evaporated to dryness and the solids were weighed. Material recovery was 98.7%, and yield of crystals was 7.62 g, or 94.4% of the theoretical yield. Calculated elemental analysis of 1-(3-methoxybenzyl)-3-dodecyl thiourea: C, 69.18; H, 9.95; N, 7.68; S, 8.79. Found: C, 69.65; H, 10.07; N, 7.67; S, 8.80.

Aufarbeitung

  1. additionpoured into a 250 ml beaker
  2. customPerforming this reaction at 40° C.
  3. stirringto stir
  4. customCrystallization
  5. temperaturestarted cooling below 50° C
  6. filtrationthe crystals were filtered off
  7. filtrationfilter paper
  8. washThe crystals were washed with 15 ml of ethanol
  9. customCombined filtrates were evaporated to dryness
  10. temperatureCooling the solution to −10° C.
  11. customgave no crystals
  12. customThe solution was evaporated to dryness

Quellen und Nachweise

ORD-Eintrag
ord-f0df843da299488baa46fd3b48aae379
Quelldatensatz
uspto-grants-2007_01
Patentnummer
US07169815B2

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