Potassium Hydroxide → HCID 22722136, compound

HRID 349173Notes

Reaction equation

HRID 349173 reaction equation
[OH-].[K+].[Cl:3][C:4]1[CH:9]=[CH:8][C:7]([CH2:10][C:11]#[N:12])=[CH:6][CH:5]=1.Cl[CH2:14][CH:15]([O:18][CH2:19][O:20][CH3:21])[CH2:16]Cl>CS(C)=O.C(OCC)C>[Cl:3][C:4]1[CH:9]=[CH:8][C:7]([C:10]2([C:11]#[N:12])[CH2:16][CH:15]([O:18][CH2:19][O:20][CH3:21])[CH2:14]2)=[CH:6][CH:5]=1

Participants

6

Procedure

Potassium hydroxide (2.57 g) was dissolved in dimethyl sulfoxide (8.0 mL). (4-Chlorophenyl)acetonitrile (1.58 g, 10.4 mmol) and 1,3-dichloro-2-(methoxymethoxy)propane (1.993 g) were dissolved in ethyl ether (3 mL), and this mixture was added dropwise to the vigorously stirred potassium hydroxide solution at room temperature. After stirring at room temperature for one hour, the reaction was quenched by adding ice-cold water (5.5 mL). The mixture was filtered through a pad of celite which was washed with ether (30 mL). The filtrate was added to a separatory funnel, and the aqueous layer was extracted with ether (3×15 mL). The organic layers were combined, dried over magnesium sulfate, filtered, and concentrated. The product was purified by silica gel chromatography to provide 1-(4-chlorophenyl)-3-(methoxymethoxy)cyclobutanecarbonitrile (1.28 g) as a mixture of isomers (ca. 2:1).

Workup

  1. customthe reaction was quenched
  2. additionby adding ice-cold water (5.5 mL)
  3. filtrationThe mixture was filtered through a pad of celite which
  4. washwas washed with ether (30 mL)
  5. additionThe filtrate was added to a separatory funnel
  6. extractionthe aqueous layer was extracted with ether (3×15 mL)
  7. dry with materialdried over magnesium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customThe product was purified by silica gel chromatography

Sources & evidence

ORD record
ord-18e6c365eed247c486bece542cd5f945
Source dataset
uspto-grants-2007_02
Patent number
US07179802B2

Reaction notes

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