Acetone → HCID 18180279, compound

HRID 1106577Notes

Reaction equation

HRID 1106577 reaction equation
[CH3:1][O:2][C:3]1[N:4]=[CH:5][C:6]2[CH2:7][CH2:8][CH2:9][C:10](=NO)[C:11]=2[CH:12]=1.CC(C)=[O:17]>Cl>[CH3:1][O:2][C:3]1[N:4]=[CH:5][C:6]2[CH2:7][CH2:8][CH2:9][C:10](=[O:17])[C:11]=2[CH:12]=1

Participants

4

Procedure

A solution of 3-methoxy-7,8-dihydro-5(6H)-isoquinolinone oxime (1.20 g, 6.25 mmol) in a mixture of acetone (40 ml) and 6M hydrochloric acid (27 ml) was refluxed for 4 h then allowed to cool to room temperature. The mixture was concentrated to remove acetone then basified with sodium carbonate and extracted four times with ethyl acetate. The combined organic extracts were dried (MgSO4), concentrated and the residue subjected to column chromatography (silica, ethyl acetate-hexane, 1:4) to afford the title compound (0.81 g) as a white solid m.p. 7981°. MS (ES+) 178 (MH+).

Workup

  1. temperaturewas refluxed for 4 h
  2. concentrationThe mixture was concentrated
  3. customto remove acetone
  4. extractionextracted four times with ethyl acetate
  5. dry with materialThe combined organic extracts were dried (MgSO4)
  6. concentrationconcentrated

Sources & evidence

ORD record
ord-6f41a51b5f284b8393aa677999a558b7
Source dataset
uspto-grants-2000_05
Patent number
US06057329

Reaction notes

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