Triacetoxyperiodinane → 2-Methoxy-4-(1-oxopropan-2-yl)benzonitrile

HRID 1474240Notes

Reaction equation

HRID 1474240 reaction equation
[OH:1][CH2:2][CH:3]([C:5]1[CH:12]=[CH:11][C:8]([C:9]#[N:10])=[C:7]([O:13][CH3:14])[CH:6]=1)[CH3:4].CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O>C(Cl)Cl>[CH3:14][O:13][C:7]1[CH:6]=[C:5]([CH:3]([CH3:4])[CH:2]=[O:1])[CH:12]=[CH:11][C:8]=1[C:9]#[N:10]

Participants

4

Reactant 2

HCID 159087TriacetoxyperiodinaneHCID 666439114-(1-Hydroxypropan-2-yl)-2-methoxybenzonitrile

Product 1

HCID 772312582-Methoxy-4-(1-oxopropan-2-yl)benzonitrile

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a stirred solution of 4-(1-hydroxypropan-2-yl)-2-methoxybenzonitrile (0.12 g, 0.63 mmol) in dry CH2Cl2 (30 mL) at 0° C. was added Dess-Martin periodinane (0.35 g, 0.82 mmol) in one portion. The mixture was stirred for 12 h at rt and quenched with a 1:1 mixture of saturated Na2S2O3 (20 mL) and saturated NaHCO3 (20 mL). The resulting mixture was diluted with CH2Cl2 (50 mL) and the layers were separated. The aqueous phase was extracted with CH2Cl2 (2×50 mL). The combined organic phases were washed with brine, dried (Na2SO4), and concentrated in vacuo to give crude 2-methoxy-4-(1-oxopropan-2-yl)benzonitrile. The crude residue was used in subsequent reactions without further purification.

Workup

  1. customquenched with a 1:1 mixture of saturated Na2S2O3 (20 mL) and saturated NaHCO3 (20 mL)
  2. additionThe resulting mixture was diluted with CH2Cl2 (50 mL)
  3. customthe layers were separated
  4. extractionThe aqueous phase was extracted with CH2Cl2 (2×50 mL)
  5. washThe combined organic phases were washed with brine
  6. dry with materialdried (Na2SO4)
  7. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-f30e17df88d84d76bd2f53d50a2390a5
Source dataset
uspto-grants-2015_04
Patent number
US09018211B2

Reaction notes

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