Ammonia → [4-(Prop-2-en-1-yloxy)phenyl]methanethiol

HRID 1392225Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1392225
[CH2:1]([O:4][C:5]1[CH:10]=[CH:9][C:8]([CH2:11]Cl)=[CH:7][CH:6]=1)[CH:2]=[CH2:3].NC(N)=[S:15].O.N>C(O)C>[CH2:1]([O:4][C:5]1[CH:10]=[CH:9][C:8]([CH2:11][SH:15])=[CH:7][CH:6]=1)[CH:2]=[CH2:3]

Komponenten

6

Edukt 4

HCID 222AmmoniaHCID 962WaterHCID 2723790ThioureaHCID 123479361-Allyloxy-4-chloromethyl-benzene

Produkt 1

HCID 22242087[4-(Prop-2-en-1-yloxy)phenyl]methanethiolAusbeute 81 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel2×

Versuchsvorschrift

A mixture of 2.00 g (10.9 mmol) 1-allyloxy-4-chloromethyl-benzene and 917 mg (12.1 mmol) thiourea in 3.0 ml ethanol was heated to reflux for 7 h. Solvents were distilled off and the crystalline residue was washed with cold ethanol and isolated by filtration. After addition of 2.5 ml ethanol, 1.0 ml water and 0.7 ml 25% aqueous ammonia, the mixture was heated to reflux for 1 h. Ethanol was distilled off, then acidified with 0.5 ml half conc. HCl and extracted with ethyl acetate. The solution was dried over MgSO4 and solvents were removed in vacuo to yield 1.59 g (81%) colourless oil, which was used immediately.

Aufarbeitung

  1. temperaturewas heated
  2. temperatureto reflux for 7 h
  3. distillationSolvents were distilled off
  4. washthe crystalline residue was washed with cold ethanol
  5. customisolated by filtration
  6. temperaturethe mixture was heated
  7. temperatureto reflux for 1 h
  8. distillationEthanol was distilled off
  9. extractionextracted with ethyl acetate
  10. dry with materialThe solution was dried over MgSO4 and solvents
  11. customwere removed in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-cc89d2b958f848ebbf09d3f40c587e8a
Quelldatensatz
uspto-grants-2008_03
Patentnummer
US07342030B2

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