2-Naphthoic acid → 2-Naphthalenecarbonyl isothiocyanate

HRID 1741143Notes

Reaction equation

HRID 1741143 reaction equation
[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]

Participants

7

Procedure

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), dhed (MgSO4), filtered and evaporated in vacuo affording 5.2 g (84%) of naphthalene-2-carbonyl isothiocyanate.

Workup

  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
  8. washThe combined organic extracts were washed with saturated aqueous sodium chloride (2×80 ml), dhed (MgSO4)
  9. filtrationfiltered
  10. customevaporated in vacuo

Sources & evidence

ORD record
ord-7716aa0498be4a9d9132aecf3cc7c084
Source dataset
uspto-grants-1999_10
Patent number
US05972978

Reaction notes

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