Methyl iodide → 4-Ethylsulfanyl-3-methoxy-3-methyl-but-1-yne

HRID 646565Notes

Reaction equation

HRID 646565 reaction equation
[CH2:1]([S:3][CH2:4][C:5]([CH3:9])([OH:8])[C:6]#[CH:7])[CH3:2].[H-].[Na+].I[CH3:13]>CN(C)C=O>[CH2:1]([S:3][CH2:4][C:5]([O:8][CH3:13])([CH3:9])[C:6]#[CH:7])[CH3:2]

Participants

5

Procedure

1-Ethylsulfanyl-2-methyl-but-3-yn-2-ol (0.29 g, 2.0 mmol) was added to a mixture of sodium hydride (60% dispersion in mineral oil, 88 mg, 2.2 mmol) in dimethylformamide (5 mL) under argon. Iodomethane (0.12 mL, 2.0 mmol) was then added to the reaction mixture via syringe and the mixture allowed to stir overnight. The mixture was poured onto water and extracted twice with diethyl ether. The diethyl ether extracts were washed with water and brine, dried over magnesium sulfate, filtered, and evaporated to yield a yellow oil. The oil was purified by column chromatography eluting with dichloromethane to yield the title compound as a clear liquid.

Workup

  1. additionThe mixture was poured onto water
  2. extractionextracted twice with diethyl ether
  3. washThe diethyl ether extracts were washed with water and brine
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. customevaporated
  7. customto yield a yellow oil
  8. customThe oil was purified by column chromatography
  9. washeluting with dichloromethane

Sources & evidence

ORD record
ord-bdc25266d2b84feeabcd22c105de5602
Source dataset
uspto-grants-2010_04
Patent number
US07705147B2

Reaction notes

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