HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Dimethylformamide → HCID 22493595, compound

HRID 1263459
Notes
Print preview

Reaction equation

HRID 1263459 reaction equation
P(Cl)(Cl)(Cl)=O.CN(C)[CH:8]=[O:9].[CH3:11][CH:12]1[CH2:21][CH2:20][CH:19]([CH3:22])[C:18]2[N:17]=[CH:16][CH:15]=[CH:14][C:13]1=2.C(=O)(O)[O-].[Na+]>C(OCC)(=O)C.CCCCCC>[CH3:11][CH:12]1[CH2:21][CH2:20][CH:19]([CH3:22])[C:18]2[NH:17][CH:16]([CH:8]=[O:9])[CH:15]=[CH:14][C:13]1=2
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 6228DimethylformamideHCID 24813Phosphorus oxychlorideHCID 516892Sodium BicarbonateHCID 22493534HCID 22493534, compound

Product 1

HCID 22493595HCID 22493595, compoundYield 59.6%

Reagents, catalysts & solvents 1

HCID 21226206
Ethyl acetate hexane
Solvent

Procedure

Phosphorus oxychloride (18.6 g, 0.12 mol) was added dropwise to 29.2 g (0.4 mol) of N,N-dimethylformamide under ice cooling. After stirring at room temperature for 30 minutes, the reaction mixture was cooled over ice bath, followed by the dropwise addition of 17.0 g (0.1 mol) of 5,8-dimethyl-5,6,7,8-tetrahydroquinoline. After stirring at room temperature for one hour, the reaction mixture was poured into ice water and neutralized with an aqueous solution of sodium bicarbonate, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue so obtained was subjected to chromatography on a silica gel column (developing solvent: 10% ethyl acetate/n-hexane), whereby 11.4 g of the title compound were obtained in the form of a reddish brown oil.

Workup

  1. temperaturethe reaction mixture was cooled over ice bath
  2. stirringAfter stirring at room temperature for one hour
  3. extractionfollowed by extraction with ethyl acetate
  4. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customThe residue so obtained

Sources & evidence

ORD record
ord-66c4e6f87e404c30a01835f3671c2bfa
Source dataset
uspto-grants-2003_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06541474B2

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes