Sodium borohydride → 5,8-dichloro-3,4-dihydroisoquinolin-1(2H)-one

HRID 577500Notes

Reaction equation

HRID 577500 reaction equation
[Cl:1][C:2]1[C:3]([CH2:14][C:15]#[N:16])=[C:4]([C:10]([Cl:13])=[CH:11][CH:12]=1)[C:5](OCC)=[O:6].[BH4-].[Na+]>C(O)C.O.O.O.O.O.O.[Co](Cl)Cl>[Cl:1][C:2]1[CH:12]=[CH:11][C:10]([Cl:13])=[C:4]2[C:3]=1[CH2:14][CH2:15][NH:16][C:5]2=[O:6]

Participants

5

Conditions

Temperature
0 °C

Procedure

Cobalt (II) chloride hexahydrate (166 g, 0.70 mol) was added to a room temperature solution of ethyl 3,6-dichloro-2-(cyanomethyl)benzoate (253d, 90 g, 0.35 mol) in ethanol (1.5 L), and the resulting mixture cooled to 0° C. Sodium borohydride (66.3 g, 1.74 mol) was added in portions. The mixture was stirred at room temperature for 1 hour, and then refluxed overnight. The resulting suspension was filtered and the filtrate concentrated in vacuo. The solids in the filter cake were stirred in ethyl acetate (600 mL), and then filtered again. This procedure was repeated a second time. The combined filtrates were added to the original filtrate residue, and this organic solution washed with water (800 mL) and saturated aqueous sodium chloride solution (800 mL), dried over sodium sulfate, and concentrated in vacuo to give 5,8-dichloro-3,4-dihydroisoquinolin-1(2H)-one (253e, 29.3 g, 39% yield) as an off-white solid.

Workup

  1. temperaturerefluxed overnight
  2. filtrationThe resulting suspension was filtered
  3. concentrationthe filtrate concentrated in vacuo
  4. stirringThe solids in the filter cake were stirred in ethyl acetate (600 mL)
  5. filtrationfiltered again
  6. additionThe combined filtrates were added to the original filtrate residue
  7. washthis organic solution washed with water (800 mL) and saturated aqueous sodium chloride solution (800 mL)
  8. dry with materialdried over sodium sulfate
  9. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-b560f9e8d4ec4b52ae736f60d3f32e92
Source dataset
uspto-grants-2015_05
Patent number
US09040515B2

Reaction notes

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