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2-Naphthoic acid → 2-Naphthalenecarbonyl isothiocyanate

HRID 619332
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 619332
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[C:11]([OH:13])=O.S(Cl)(Cl)=O.[S-:18][C:19]#[N:20].[K+]>CN(C=O)C.O1CCCC1.CC(C)=O>[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[C:11]([N:20]=[C:19]=[S:18])=[O:13]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 3

HCID 71232-Naphthoic acidHCID 24386Thionyl ChlorideHCID 516872Potassium thiocyanate

Produkt 1

HCID 21134132-Naphthalenecarbonyl isothiocyanateAusbeute 84,1 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 6228DimethylformamideKatalysatorHCID 180
Acetone
Lösungsmittel
HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To a mixture of 2-naphthyl carboxylic acid (5.0 g, 29.0 mmol) and 2 drops of N,N'-dimethylformamide in dry tetrahydrofuran (50 ml) was added dropwise thionyl chloride (6.3 ml, 87 mmol) and the resulting reaction mixture was stirred at reflux temperature for 3 h. The volatiles were evaporated in vacuo and the solid residue was redissolved in dry tetrahydrofuran (30 ml) and added dropwise to a solution of potassium thiocyanate (2.9 g, 30 mmol) in acetone (40 ml). The reaction mixture was stirred at room temperature for 16 h. The reaction mixture was quenched with water (250 ml) and extracted with diethyl ether (2×100 ml). The combined organic extracts were washed with saturated aqueous sodium chloride (2×80 ml), dried (MgSO4), filtered and evaporated in vacuo affording 5.2 g (84%) of naphthalene-2-carbonyl isothiocyanate.

Aufarbeitung

  1. customthe resulting reaction mixture
  2. temperatureat reflux temperature for 3 h
  3. customThe volatiles were evaporated in vacuo
  4. dissolutionthe solid residue was redissolved in dry tetrahydrofuran (30 ml)
  5. stirringThe reaction mixture was stirred at room temperature for 16 h
  6. customThe reaction mixture was quenched with water (250 ml)
  7. extractionextracted with diethyl ether (2×100 ml)
  8. washThe combined organic extracts were washed with saturated aqueous sodium chloride (2×80 ml)
  9. dry with materialdried (MgSO4)
  10. filtrationfiltered
  11. customevaporated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-62d97194fc01438ab9085bedb0797a81
Quelldatensatz
uspto-grants-1999_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05958957

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