Water → 1-(2,5-Dichlorophenyl)-3-(1-methyl-2-pyrrolidylidene)urea

HRID 2071500

Reaction equation

HRID 2071500 reaction equation
Cl.[CH3:2][N:3]1[CH2:7][CH2:6][CH2:5][C:4]1=[NH:8].O.[OH-].[Na+].[Cl:12][C:13]1[CH:18]=[CH:17][C:16]([Cl:19])=[CH:15][C:14]=1[N:20]=[C:21]=[O:22]>C1C=CC=CC=1>[Cl:12][C:13]1[CH:18]=[CH:17][C:16]([Cl:19])=[CH:15][C:14]=1[NH:20][C:21]([N:8]=[C:4]1[CH2:5][CH2:6][CH2:7][N:3]1[CH3:2])=[O:22]

Participants

6

Reactant 4

HCID 962WaterHCID 14798Sodium HydroxideHCID 79360Benzene, 1,4-dichloro-2-isocyanato-HCID 124489671-Methylpyrrolidin-2-imine hydrochloride

Product 1

HCID 542302811-(2,5-Dichlorophenyl)-3-(1-methyl-2-pyrrolidylidene)urea

Reagents, catalysts & solvents 1

HCID 241BenzeneSolvent

Procedure

To 6.73 g. (0.05 mole) of 1-methyl-2-iminopyrrolidine HCl is added 1 ml. of water and 50 ml. of benzene. After solution is complete (magnetic stirring), 10 ml. of aqueous sodium hydroxide (50%) is added in one portion. After stirring for about 1 min., the benzene layer is decanted onto anhydrous potassium carbonate. The extraction is repeated twice. After drying (occasional swirling) the combined benzene extracts are filtered (dicalite) from drying agent and 9.4 g. (0.05 mole) of 2,5-dichlorophenylisocyanate is added to the filtrate in one portion with swirling. After stirring for 3 hours, the solvent is removed in vacuo affording a colorless solid, 1-(2,5-dichlorophenyl)-3-(1-methyl-2-pyrrolidylidene)urea. Recrystallization from acetone (twice) yields the pure product, m.p. = 148.5°-150.5° C.

Workup

  1. stirringAfter stirring for about 1 min.
  2. customthe benzene layer is decanted onto anhydrous potassium carbonate
  3. extractionThe extraction
  4. dry with materialAfter drying (occasional swirling) the combined benzene extracts
  5. filtrationare filtered (dicalite)
  6. customfrom drying agent and 9.4 g
  7. stirringAfter stirring for 3 hours
  8. customthe solvent is removed in vacuo

Sources & evidence

ORD record
ord-4abd23e35fd1426ea75e859d24fda9f4
Source dataset
uspto-grants-1977_09
Patent number
US04046909

Linked notes

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