Potassium thiocyanate → HCID 20387432, compound

HRID 1438804Notes

Reaction equation

HRID 1438804 reaction equation
Cl.Cl[CH2:3][CH2:4][S:5][CH2:6][C:7]1[N:8]=[CH:9][NH:10][C:11]=1[CH3:12].[S-:13][C:14]#[N:15].[K+]>C(O)C>[CH3:12][C:11]1[NH:10][CH:9]=[N:8][C:7]=1[CH2:6][S:5][CH2:4][CH2:3][S:13][C:14]#[N:15]

Participants

4

Reactant 2

HCID 516872Potassium thiocyanateHCID 132173611-Chloro-2(5-methyl-4-imidazolylmethylthio)ethane hydrochloride

Product 1

HCID 20387432HCID 20387432, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

1-Chloro-2-(5-methyl-4-imidazolylmethylthio)ethane hydrochloride (2.1 g) and potassium thiocyanate (0.97 g) were heated together under reflux in ethanol (50 ml) for 3 days. The mixture was evaporated to dryness and the residue was taken up in water, basified with sodium carbonate and extracted with chloroform. The chloroform extracts were dried (MgSO4) and evaporated to a residue which was recrystallised from acetonitrile to give 2-(5-methyl-4-imidazolylmethylthio)ethylthiocyanate m.p. 101°-103°.

Workup

  1. customThe mixture was evaporated to dryness
  2. extractionextracted with chloroform
  3. dry with materialThe chloroform extracts were dried (MgSO4)
  4. customevaporated to a residue which
  5. customwas recrystallised from acetonitrile

Sources & evidence

ORD record
ord-9c59b5a8b33a4912a5f8a8770a69c154
Source dataset
uspto-grants-1977_11
Patent number
US04056621

Reaction notes

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