Sulfuric Acid → HCID 53827548, compound

HRID 259736Notes

Reaction equation

HRID 259736 reaction equation
S(=O)(=O)(O)O.[CH:6]([C:9]([CH3:27])([N:12]1[C:16](=[O:17])[C:15]2[CH:18]=[CH:19][C:20]3[N:21]([CH3:25])[CH:22]=[CH:23][C:24]=3[C:14]=2[C:13]1=[O:26])[C:10]#[N:11])([CH3:8])[CH3:7].[OH-].[Na+].CC[O:32]CC>C(Cl)Cl.C(OCC)(=O)C>[CH:6]([C:9]([CH3:27])([N:12]1[C:16](=[O:17])[C:15]2[CH:18]=[CH:19][C:20]3[N:21]([CH3:25])[CH:22]=[CH:23][C:24]=3[C:14]=2[C:13]1=[O:26])[C:10]([NH2:11])=[O:32])([CH3:8])[CH3:7]

Participants

7

Procedure

Concentrated sulfuric acid (5.50 mL) is added slowly to a solution of 3,6-dihydro-α-isopropyl-α,6-dimethyl-1,3-dioxobenzo[1,2-b:3,4-c']dipyrrole-2(1H)-acetonitrile (5.50 g, 19.0 mmol) in methylene chloride at 10° C. Crushed ice is added. The mixture is stirred for 24 hours at ambient temperature and poured onto crushed ice, treated with 6N sodium hydroxide to pH 2, and extracted with methylene chloride. The organic layer is separated, dried (MgSO4) and concentrated in vacuo to give an orange foamy residue. Flash chromatography (silica gel, ether then ethyl acetate eluents) affords the title product as a yellow foam (1.53 g, 25.7%), mp 159°-168° C.

Workup

  1. additionCrushed ice is added
  2. additionpoured
  3. customonto crushed ice
  4. extractionextracted with methylene chloride
  5. customThe organic layer is separated
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated in vacuo
  8. customto give an orange foamy residue

Sources & evidence

ORD record
ord-1c3c34bfecf64df485557939602d2d56
Source dataset
uspto-grants-1996_06
Patent number
US05523279

Reaction notes

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