Carbon Dioxide → HCID 10953610, compound

HRID 1389124Notes

Reaction equation

HRID 1389124 reaction equation
[NH:1]1[CH:5]=[CH:4][CH:3]=[CH:2]1.N[C:7](N)=[S:8].[I-].[K+].II.[CH2:14](I)[CH2:15]C.[OH-].[K+].C(=O)=O.[Cl-].[Na+]>C(O)C.O.CO>[CH2:7]([S:8][C:2]1[NH:1][CH:5]=[CH:4][CH:3]=1)[CH2:14][CH3:15]

Participants

12

Procedure

A mixture of pyrrole (6.7 g., 0.10 mole) and thiourea (7.6 g., 0.10 mole) in 50% aqueous ethanol (500 ml.) was stirred at room temperature under nitrogen while a solution of potassium iodide (16.6 g., 0.10 mole) and iodine (12.7 g., 0.05 mole) in water (100 ml.) was added dropwise. The solution was cooled to 0° and a solution of propyl iodide (18 g., 0.105 mole) in methanol (20 ml.) was added followed by the dropwise addition of a solution of potassium hydroxide (5.6 g.) in 50% aqueous methanol (40 ml.). The mixture was stirred for a further 1.5 hours at room temperature and the solution then neutralized by the addition of solid carbon dioxide. The reaction mixture was poured into a solution of sodium chloride (25 g.) in water (100 ml.) and the solution extracted with methylene chloride (3×50 ml.). The organic extracts were combined, dried over sodium sulphate and the solvent evaporated to give an oil which was distilled under reduced pressure to yield 2-n-propylthiopyrrole (1.0 g.), B.P. 115° at 15 mm.

Workup

  1. additionwas added dropwise
  2. temperatureThe solution was cooled to 0°
  3. extractionthe solution extracted with methylene chloride (3×50 ml.)
  4. dry with materialdried over sodium sulphate
  5. customthe solvent evaporated
  6. customto give an oil which
  7. distillationwas distilled under reduced pressure

Sources & evidence

ORD record
ord-f101f86660574b119a718d17dcdf4ea8
Source dataset
uspto-grants-1981_01
Patent number
US04243672

Reaction notes

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