Phosphorus oxychloride → Ethyl 4,5-dihydro-2-methyl-8-methylthiothieno[3,4-g]benzoxazole-6-carboxylate

HRID 2296802Notes

Reaction equation

HRID 2296802 reaction equation
[C:1]([NH:4][CH:5]1[CH2:20][CH2:19][C:8]2=[C:9]([C:14]([O:16][CH2:17][CH3:18])=[O:15])[S:10][C:11]([S:12][CH3:13])=[C:7]2[C:6]1=[O:21])(=O)[CH3:2].P(Cl)(Cl)(Cl)=O>C1(C)C=CC=CC=1>[CH3:2][C:1]1[O:21][C:6]2[C:7]3=[C:11]([S:12][CH3:13])[S:10][C:9]([C:14]([O:16][CH2:17][CH3:18])=[O:15])=[C:8]3[CH2:19][CH2:20][C:5]=2[N:4]=1

Participants

4

Reactant 2

HCID 24813Phosphorus oxychlorideHCID 12043499Ethyl 5-acetylamino-4,5,6,7-tetrahydro-3-methylthio-4-oxobenzo[c]thiophene-1-carboxylate

Product 1

HCID 12043502Ethyl 4,5-dihydro-2-methyl-8-methylthiothieno[3,4-g]benzoxazole-6-carboxylateYield 94%

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

A mixture of ethyl 5-acetylamino-4,5,6,7-tetrahydro-3-methylthio-4-oxobenzo[c]thiophene-1-carboxylate (2.46 g), phosphorus oxychloride (3.46 g) and toluene (80 ml) was refluxed under heating for 1.5 hours; the solution obtained was concentrated under reduced pressure, diluted with a saturated aqueous solution of sodium hydrogen carbonate (200 ml) and extracted with ethyl acetate. The organic layer was washed with water and dried (MgSO4), after which the solvent was distilled off to yield ethyl 4,5-dihydro-2-methyl-8-methylthiothieno[3,4-g]benzoxazole-6-carboxylate (2.18 g, 94.0%), which was then recrystallized from ethyl acetate-hexane. Light-yellow needles. Melting point 131-132° C.

Workup

  1. temperaturewas refluxed
  2. temperatureunder heating for 1.5 hours
  3. customthe solution obtained
  4. concentrationwas concentrated under reduced pressure
  5. additiondiluted with a saturated aqueous solution of sodium hydrogen carbonate (200 ml)
  6. extractionextracted with ethyl acetate
  7. washThe organic layer was washed with water
  8. dry with materialdried (MgSO4)
  9. distillationafter which the solvent was distilled off

Sources & evidence

ORD record
ord-5304e07a76ca4f7b9baaa4cef4db616f
Source dataset
uspto-grants-2002_12
Patent number
US06489351B1

Reaction notes

Loading…