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Methyl iodide → 2-[4-(Propan-2-yl)phenyl]propanenitrile

HRID 720550
Notes
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Reaction equation

HRID 720550 reaction equation
[CH:1]([C:4]1[CH:9]=[CH:8][C:7]([CH2:10][C:11]#[N:12])=[CH:6][CH:5]=1)([CH3:3])[CH3:2].[CH3:13][Si]([N-][Si](C)(C)C)(C)C.[Li+].IC>O1CCCC1>[CH:1]([C:4]1[CH:5]=[CH:6][C:7]([CH:10]([CH3:13])[C:11]#[N:12])=[CH:8][CH:9]=1)([CH3:3])[CH3:2]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 6328Methyl iodideHCID 1382224-IsopropylphenylacetonitrileHCID 2733832Lithium hexamethyldisilazane

Product 1

HCID 136820102-[4-(Propan-2-yl)phenyl]propanenitrileYield 73%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Conditions

Temperature
-78 °C

Procedure

In a 250 ml flask, 4-isopropylphenylacetonitrile 8.00 g (50.2 mmol) was dissolved in tetrahydrofuran (150 ml) under a nitrogen atmosphere. The solution was cooled to −78° C. and lithium bis(trimethylsilyl)amide (1M in tetrahydrofuran, 52.8 ml (52.8 mmol) added. The resulting mixture was stirred at −78° C. for 1 hour. To this reaction mixture was added iodomethane 3.29 ml (52.8 mmol). The resulting mixture was slowly allowed to warm to ambient temperature over 16 hours then quenched with 0.2M hydrochloric acid and extracted twice with diethyl ether. The organic fractions were combined, dried (MgSO4) and concentrated under vacuo. Chromatography (SiO2, 20% ethyl acetate/hexanes) gave 6.32 g (73%) of the title compound.

Workup

  1. temperatureto warm to ambient temperature over 16 hours
  2. customthen quenched with 0.2M hydrochloric acid
  3. extractionextracted twice with diethyl ether
  4. dry with materialdried (MgSO4)
  5. concentrationconcentrated under vacuo

Sources & evidence

ORD record
ord-46df4c6e30f74d1a813ac9275cd68f9c
Source dataset
uspto-grants-2006_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07135487B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes