N,N-Diethylaniline → HCID 178503469, compound

HRID 1359438Notes

Reaction equation

HRID 1359438 reaction equation
[CH3:1][S:2][C:3]1[NH:4][C:5]2[C:6]([N:10]=[CH:11][CH:12]=2)=[C:7](O)[N:8]=1.C(N(CC)C1C=CC=CC=1)C.P(Cl)(Cl)([Cl:26])=O>>[CH3:1][S:2][C:3]1[NH:4][C:5]2[C:6]([N:10]=[CH:11][CH:12]=2)=[C:7]([Cl:26])[N:8]=1

Participants

4

Procedure

Compound (3.2) (8.7 g, 48 mmol) was mixed with phosphorus oxychloride (350 ml) and N,N-diethylaniline (17.5 ml). This mixture was heated under reflux for 4 hrs; the brown solution was then concentrated under reduced pressure. The residual oil was treated with an ice-water mixture and stirred until the ice had melted. The resultant mixture was extracted repeatedly with ether until no more UV-active material was being extracted, the combined aqueous extracts were dried (MgSO4), filtered and evaporated to a light beige solid. Dried under vacuum at 50° C. to give (3.3), 7.3 g (76%). δH (300 MHz, DMSO-d6) 1.78 (3H, s, SCH3), 5.70 (1 H, d, J 3.7 Hz, H7) and 6.51 (1H, d, J 3.7 Hz, H8) ppm.

Workup

  1. temperatureThis mixture was heated
  2. temperatureunder reflux for 4 hrs
  3. concentrationthe brown solution was then concentrated under reduced pressure
  4. additionThe residual oil was treated with an ice-water mixture
  5. extractionThe resultant mixture was extracted repeatedly with ether until no more UV-active material
  6. extractionwas being extracted
  7. dry with materialthe combined aqueous extracts were dried (MgSO4)
  8. filtrationfiltered
  9. customevaporated to a light beige solid
  10. customDried under vacuum at 50° C.

Sources & evidence

ORD record
ord-327809f713f942a49c97529dc342c700
Source dataset
uspto-grants-2003_07
Patent number
US06600028B1

Reaction notes

Loading…