Ethyl Acetate → HCID 66745877, compound

HRID 2410165Notes

Reaction equation

HRID 2410165 reaction equation
[CH:1]1([O:7][C:8]2[CH:15]=[CH:14][CH:13]=[C:12]([N+:16]([O-])=O)[C:9]=2[C:10]#[N:11])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.CCOC(C)=O>C1COCC1.CC(O)=O.[Fe]>[NH2:16][C:12]1[CH:13]=[CH:14][CH:15]=[C:8]([O:7][CH:1]2[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]2)[C:9]=1[C:10]#[N:11]

Participants

5

Procedure

To a solution of 2-(cyclohexyloxy)-6-nitrobenzonitrile (Example Hc, 50.0 g, 0.20 mol) in THF/AcOH (1:1 by volume, 500 mL) was added iron powder (34.0 g, 0.61 mol) in one portion at room temperature under nitrogen. The reaction mixture was refluxed for 40 min under nitrogen and cooled down to room temperature and EtOAc (2 L) was added. The precipitate that formed was filtered off and washed with EtOAc. The organic layer was separated and washed successively with water (2×300 mL), aqueous NaOH (1.0 N, 2×300 mL), saturated Na2CO3 solution (300 mL), brine (300 mL), dried over Na2SO4 filtered and evaporated under reduced pressure. The residue was purified by chromatography on silica gel eluting with 25% EtOAc in hexanes to give 2-amino-6-(cyclohexyloxy)benzonitrile as a pale yellow oil (45.0 g, 94%), which solidified after storage overnight at room temperature.

Workup

  1. customat room temperature
  2. temperatureThe reaction mixture was refluxed for 40 min under nitrogen
  3. customThe precipitate that formed
  4. filtrationwas filtered off
  5. washwashed with EtOAc
  6. customThe organic layer was separated
  7. washwashed successively with water (2×300 mL), aqueous NaOH (1.0 N, 2×300 mL), saturated Na2CO3 solution (300 mL), brine (300 mL)
  8. dry with materialdried over Na2SO4
  9. filtrationfiltered
  10. customevaporated under reduced pressure
  11. customThe residue was purified by chromatography on silica gel eluting with 25% EtOAc in hexanes

Sources & evidence

ORD record
ord-ed0ac44e60684a8d99734488eb9982af
Source dataset
uspto-grants-2014_08
Patent number
US08815956B2

Reaction notes

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