p-Toluenesulfonic acid → HCID 15018890, compound

HRID 1709108Notes

Reaction equation

HRID 1709108 reaction equation
[CH2:1]([C:4]1[CH:9]=[CH:8][C:7]([N:10]2[C:14](=[O:15])[C:13]3[CH2:16][CH2:17][CH2:18][CH2:19][C:12]=3[C:11]2=[O:20])=[CH:6][C:5]=1[OH:21])[CH:2]=[CH2:3].C1(C)C=CC(S(O)(=O)=O)=CC=1.C(=O)(O)[O-].[Na+]>C1(C)C(C)=CC=CC=1>[CH3:3][CH:2]1[CH2:1][C:4]2[CH:9]=[CH:8][C:7]([N:10]3[C:11](=[O:20])[C:12]4[CH2:19][CH2:18][CH2:17][CH2:16][C:13]=4[C:14]3=[O:15])=[CH:6][C:5]=2[O:21]1

Participants

5

Procedure

A mixture of 0.20 g of 1C, 100 mg of p-toluenesulfonic acid (PTSA), and 10 mL of xylene was refluxed for 24 hours, then cooled and poured into a saturated aqueous solution of sodium bicarbonate. The resulting mixture was extracted with ethyl acetate, and the extract was washed in succession with sodium bicarbonate solution, water and brine, dried (Na2SO4) and filtered. The solvent was evaporated and the residue was chromatographed on a Chromatotron™ plate, starting with a 3:17 v:v mixture of ethyl acetate and hexane as eluent and gradually increasing the ethyl acetate content in the eluent, to give the title compound, as yellow crystals, m.p.: 114°-118° C.

Workup

  1. temperaturewas refluxed for 24 hours
  2. temperaturecooled
  3. extractionThe resulting mixture was extracted with ethyl acetate
  4. washthe extract was washed in succession with sodium bicarbonate solution, water and brine
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. customThe solvent was evaporated
  8. customthe residue was chromatographed on a Chromatotron™ plate
  9. additionv mixture of ethyl acetate and hexane as eluent
  10. temperaturegradually increasing the ethyl acetate content in the eluent

Sources & evidence

ORD record
ord-5f6b8393a8ba40459f1ff7b0f41edbe0
Source dataset
uspto-grants-1990_08
Patent number
US04948418

Reaction notes

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