Potassium thiocyanate → 4-Tert-butyl-1,3-dihydroimidazole-2-thione

HRID 1679671Notes

Reaction equation

HRID 1679671 reaction equation
Cl.[NH2:2][CH2:3][C:4](=O)[C:5]([CH3:8])([CH3:7])[CH3:6].[S-:10][C:11]#[N:12].[K+]>O>[C:5]([C:4]1[N:12]=[C:11]([SH:10])[NH:2][CH:3]=1)([CH3:8])([CH3:7])[CH3:6]

Participants

4

Reactant 2

HCID 516872Potassium thiocyanateHCID 221479671-Amino-3,3-dimethylbutan-2-one hydrochloride

Product 1

HCID 1784413604-Tert-butyl-1,3-dihydroimidazole-2-thione

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

35.2 g. 1-Amino-3,3-dimethylbutan-2-one hydrochloride and 30 g. potassium thiocyanate in 50 ml. water was warmed on the steam bath for two hours. After cooling, the solid formed was collected, washed with water, dried and recrystallised from industrial methylated spirit to give 4-tert.butylimidazole-2-thiol, melting point 232°-234° C. A solution/suspension of this in industrial methylated spirit was added to a solution of 4.5 g. sodium hydroxide in 100 ml. water. 17.6 g. Ethyl iodide was added forming a lower layer and the mixture was shaken for two minutes whilst the ethyl iodide reacted and dispersed. After 20 minutes the alkali was neutralised by passing in carbon dioxide and the methylated spirit removed by evaporation. The solid was collected, washed with water, dried and on recrystallisation from toluene gave 2-ethylthio-4-tert.butylimidazole, melting point 116.5°-120° C.

Workup

  1. temperatureAfter cooling
  2. customthe solid formed
  3. customwas collected
  4. washwashed with water
  5. customdried
  6. customrecrystallised from industrial methylated spirit

Sources & evidence

ORD record
ord-845a8f7acb8a4e16998abbb3cbdabb90
Source dataset
uspto-grants-1978_03
Patent number
US04081540

Reaction notes

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