Diethyl Ether → HCID 18919381, compound

HRID 1450364Notes

Reaction equation

HRID 1450364 reaction equation
C(N(CC)CC)C.[O:8]=[C:9]([N:12]([C:30](=[O:33])[CH2:31][CH3:32])[C:13]1[C:18]([S:19](O)(=[O:21])=[O:20])=[CH:17][CH:16]=[CH:15][C:14]=1[C:23]1[CH:28]=[CH:27][CH:26]=[C:25]([CH3:29])[CH:24]=1)[CH2:10][CH3:11].P(Cl)(Cl)(Cl)(Cl)[Cl:35].CCOCC>ClCCl>[O:8]=[C:9]([N:12]([C:30](=[O:33])[CH2:31][CH3:32])[C:13]1[C:18]([S:19]([Cl:35])(=[O:21])=[O:20])=[CH:17][CH:16]=[CH:15][C:14]=1[C:23]1[CH:28]=[CH:27][CH:26]=[C:25]([CH3:29])[CH:24]=1)[CH2:10][CH3:11]

Participants

6

Procedure

To a solution of 3.6 g (7.6 retool) of the N,N-diethylethanamine salt of 2-[bis(1-oxopropyl)amino]-3'-methyl [1,1'-biphenyl]-3-sulphonic acid in 8 ml of dichloromethane, at 0° C., are added 1.6 g (7.6 mmol) of phosphorus pentachloride and the mixture is allowed to return to room temperature. The mixture is then heated for 4 hours at the reflux temperature and is then allowed to return to room temperature. Ether is added, the mixture is filtered, the filtrate is concentrated and the residue is purified on a column of florisil™, eluting with an ether/pentane mixture (1/1). The product is recrystallized from an ether/pentane mixture.

Workup

  1. customto return to room temperature
  2. temperatureThe mixture is then heated for 4 hours at the reflux temperature
  3. customto return to room temperature
  4. filtrationthe mixture is filtered
  5. concentrationthe filtrate is concentrated
  6. customthe residue is purified on a column of florisil™
  7. washeluting with an ether/pentane mixture (1/1)
  8. customThe product is recrystallized from an ether/pentane mixture

Sources & evidence

ORD record
ord-34d9191d150740cbaad01233a80f28bf
Source dataset
uspto-grants-1997_02
Patent number
US05602149

Reaction notes

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