2-Chlorobenzoyl chloride → HCID 13457735, compound

HRID 462742Notes

Reaction equation

HRID 462742 reaction equation
[C:1]1(=[O:16])[N:5]([N:6]2[CH:10]=[CH:9][CH:8]=[CH:7]2)[C:4](=[O:11])[C:3]2=[CH:12][CH:13]=[CH:14][CH:15]=[C:2]12.[Cl:17][C:18]1[CH:26]=[CH:25][CH:24]=[CH:23][C:19]=1[C:20](Cl)=[O:21]>ClCCCl>[Cl:17][C:18]1[CH:26]=[CH:25][CH:24]=[CH:23][C:19]=1[C:20]([C:7]1[N:6]([N:5]2[C:4](=[O:11])[C:3]3=[CH:12][CH:13]=[CH:14][CH:15]=[C:2]3[C:1]2=[O:16])[CH:10]=[CH:9][CH:8]=1)=[O:21]

Participants

4

Reactant 2

HCID 691102-Chlorobenzoyl chlorideHCID 8537192-(1H-Pyrrol-1-yl)isoindoline-1,3-dione

Product 1

HCID 13457735HCID 13457735, compoundYield 123.7%

Reagents, catalysts & solvents 1

HCID 111,2-DichloroethaneSolvent

Procedure

To a vigorously stirred mixture of 1-phthalimidopyrrole (45 g, 0.212 mol) and o-chlorobenzoyl chloride (37 g, 0.212 mole) in 500 ml of 1,2-dichloroethane was added freshly pulverized, fused zinc chloride (43.3 g, 0.318 mol) in one portion. The reaction mixture was heated at gentle reflux for 4.5 hours and then quenched with 700 ml of crushed ice and 500 ml of dichloromethane. The organic layer was separated and washed with water (2×500 ml), dried over anhydrous MgSO4, filtered, and evaporated to give 92 g of an oil. This oil was purified by column chromatography (silica gel/dichloromethane) to give 33.8 g (45%) of needles, m.p. 158°-160° C.

Workup

  1. additionwas added freshly
  2. temperatureThe reaction mixture was heated
  3. temperatureat gentle reflux for 4.5 hours
  4. customquenched with 700 ml of crushed ice and 500 ml of dichloromethane
  5. customThe organic layer was separated
  6. washwashed with water (2×500 ml)
  7. dry with materialdried over anhydrous MgSO4
  8. filtrationfiltered
  9. customevaporated

Sources & evidence

ORD record
ord-ba3801e3900a4853a23cb6640d077d3b
Source dataset
uspto-grants-1985_05
Patent number
US04517195

Reaction notes

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