Benzene → 1-(1-Methyl-2-pyrrolidylidene)-3-p-tolylurea

HRID 2071492

Reaktionsgleichung

Reaktionsgleichung von HRID 2071492
Cl.[CH3:2][N:3]1[CH2:7][CH2:6][CH2:5][C:4]1=[NH:8].C1C=CC=CC=1.[OH-].[Na+].[C:17]1([CH3:26])[CH:22]=[CH:21][C:20]([N:23]=[C:24]=[O:25])=[CH:19][CH:18]=1>O>[CH3:2][N:3]1[CH2:7][CH2:6][CH2:5][C:4]1=[N:8][C:24]([NH:23][C:20]1[CH:21]=[CH:22][C:17]([CH3:26])=[CH:18][CH:19]=1)=[O:25]

Komponenten

6

Versuchsvorschrift

To a suspension of 6.73 g. (0.05 mole) of 1-methyl-2-iminopyrrolidine hydrochloride in 100 ml. of benzene is added 2 ml. of water followed by 5 ml. of 50% NaOH. After stirring for 5 min., the benzene layer is decanted onto anhydrous potassium carbonate. The extraction is repeated twice with 75 ml. portions of fresh benzene. The combined extracts are filtered from drying agent (dicalite pad and suction). To the filtrate is added in one portion with stirring 6.66 g. (0.05 mole) of p-tolylisocyanate. After stirring for 5 hours, the solution is taken to dryness in vacuo and the resulting solid is recrystallized from ethyl acetate to give 1-(1-methyl-2-pyrrolidylidene)-3-p-tolylurea, m.p. = 136°-137° C. A final recrystallization from acetone shows the product melting at 140°-150° C. Thin layer chromatography (TLC) indicates both samples to be identical in purity. Apparently the two melting points represent polymorphic forms.

Aufarbeitung

  1. additionTo a suspension of 6.73 g
  2. customthe benzene layer is decanted onto anhydrous potassium carbonate
  3. extractionThe extraction
  4. filtrationThe combined extracts are filtered
  5. dry with materialfrom drying agent (dicalite pad and suction)
  6. additionTo the filtrate is added in one portion
  7. stirringwith stirring 6.66 g
  8. stirringAfter stirring for 5 hours
  9. customthe resulting solid is recrystallized from ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-51f3f17d9dad4782925c63830e5b9f00
Quelldatensatz
uspto-grants-1977_09
Patentnummer
US04046909

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