N,N-Diethylaniline → HCID 178503469, compound
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]=1Participants
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
- temperatureThis mixture was heated
- temperatureunder reflux for 4 hrs
- concentrationthe brown solution was then concentrated under reduced pressure
- additionThe residual oil was treated with an ice-water mixture
- extractionThe resultant mixture was extracted repeatedly with ether until no more UV-active material
- extractionwas being extracted
- dry with materialthe combined aqueous extracts were dried (MgSO4)
- filtrationfiltered
- customevaporated to a light beige solid
- customDried under vacuum at 50° C.
Sources & evidence
- ORD record
- ord-327809f713f942a49c97529dc342c700
- Source dataset
- uspto-grants-2003_07
- Patent number
- US06600028B1
Reaction notes
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