Cyclohexanecarboxamide → Cyclohexanecarbothioamide
Reaction equation
[CH:1]1([C:7]([NH2:9])=O)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.P12(SP3(SP(SP(S3)(S1)=S)(=S)S2)=S)=[S:11].C(=O)(O)[O-].[Na+]>C1(C)C=CC=CC=1>[CH:1]1([C:7](=[S:11])[NH2:9])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 115 °C
Procedure
25.0 g Cyclohexanecarboxamide were dissolved in 200 ml toluene. 8.74 g phosphorus pentasulfide were added, followed by the addition of 33.0 g sodium bicarbonate. The reaction mixture was warmed to 115° C. and stirred overnight. The reaction mixture was filtered over a celite pad, washed with dichloromethane. The filtrate evaporated under reduced pressure. The residue was dissolved in 250 ml dichloromethane and the organic layer was washed three times with 100 ml water and twice with 100 ml brine. The aqueous layer was extracted five times with 100 ml dichloromethane. The combined organic layers were dried over MgSO4 and the solvent removed under reduced pressure. The resulting residue was purified by chromatography with the eluent dichloromethane:ethyl acetate=1:1 to obtain 7.92 g Cyclohexanecarbothioic acid amide as a yellow solid.
Workup
- filtrationThe reaction mixture was filtered over a celite pad
- washwashed with dichloromethane
- customThe filtrate evaporated under reduced pressure
- dissolutionThe residue was dissolved in 250 ml dichloromethane
- washthe organic layer was washed three times with 100 ml water
- extractionThe aqueous layer was extracted five times with 100 ml dichloromethane
- dry with materialThe combined organic layers were dried over MgSO4
- customthe solvent removed under reduced pressure
- customThe resulting residue was purified by chromatography with the eluent dichloromethane
Sources & evidence
- ORD record
- ord-259f9a67bf6b41d9b3f7618f713f9976
- Source dataset
- uspto-grants-2010_05
- Patent number
- US07709481B2
Reaction notes
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