Diphenylmethane → 6-Ethoxyisoquinolin-1(2H)-one

HRID 1821600Notes

Reaction equation

HRID 1821600 reaction equation
ClC([O:4][CH2:5]C)=O.[CH2:7]([O:9][C:10]1[CH:11]=[C:12]([CH:18]=[CH:19][CH:20]=1)[CH:13]=[CH:14]C(O)=O)[CH3:8].C([N:23](CC)CC)C.[N-]=[N+]=[N-].[Na+].C1(CC2C=CC=CC=2)C=CC=CC=1.C(N(CCCC)CCCC)CCC>CC(C)=O.O>[CH2:7]([O:9][C:10]1[CH:11]=[C:12]2[C:18](=[CH:19][CH:20]=1)[C:5](=[O:4])[NH:23][CH:14]=[CH:13]2)[CH3:8]

Participants

9

Conditions

Temperature
23 °C

Procedure

Ethyl chloroformate (4.3 mL, 44.5 mmol) was added drop wise at 0° C. to a solution of 3-Ethoxy cinnamic acid (5.71 g, 29.7 mmol) and triethylamine (8.3 mL, 59.4 mmol) in acetone (35 mL). After 1 h at 0° C., aqueous sodium azide (3.1 g, 47.5 mmol, 16 mL water) was added dropwise and the reaction mixture was stirred at 23° C. for 16 h. Water (50 mL) was added to the mixture and the volatile was removed under vacuo. The resulting slurry was extracted with toluene (3×25 mL) and the combined organic layers were dried (MgSO4). The dried solution was filtered and added dropwise at 190° C. to a solution of diphenylmethane (25 mL) and tributylamine (14.2 mL, 59.4 mmol). The toluene was distilled off as added. After complete addition, the reaction temperature was raised to 210° C. for 2 h. After cooling, the precipitated product was collected by filtration and washed with hexanes and dried under vacuum to yield 6-Ethoxy-2H-isoquinolin-1-one (1.92 g, 10.2 mmol, 34% yield). MS m/z 190 (M++H).

Workup

  1. customthe volatile was removed under vacuo
  2. extractionThe resulting slurry was extracted with toluene (3×25 mL)
  3. dry with materialthe combined organic layers were dried (MgSO4)
  4. filtrationThe dried solution was filtered
  5. distillationThe toluene was distilled off
  6. additionas added
  7. additionAfter complete addition
  8. temperaturethe reaction temperature was raised to 210° C. for 2 h
  9. temperatureAfter cooling
  10. filtrationthe precipitated product was collected by filtration
  11. washwashed with hexanes
  12. customdried under vacuum

Sources & evidence

ORD record
ord-94ec03d0e49e40548bfdf0a98c9bf204
Source dataset
uspto-grants-2009_10
Patent number
US07608592B2

Reaction notes

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