Methyl iodide → Ethyl 1-methyl-1-(4-methylphenyl)ethanesulfonate

HRID 1005394Notes

Reaction equation

HRID 1005394 reaction equation
[CH2:1]([Li])[CH2:2][CH2:3]C.CC1C=C[C:10]([CH2:13][S:14]([O:17][CH2:18][CH3:19])(=[O:16])=[O:15])=CC=1.I[CH3:21].[CH2:22]1[CH2:26]O[CH2:24][CH2:23]1>>[CH3:21][C:13]([C:22]1[CH:23]=[CH:24][C:2]([CH3:3])=[CH:1][CH:26]=1)([S:14]([O:17][CH2:18][CH3:19])(=[O:15])=[O:16])[CH3:10]

Participants

5

Reactant 4

HCID 6328Methyl iodide2×HCID 8028Tetrahydrofuran2×HCID 12456502Ethyl 4-methylphenylmethanesulfonateHCID 178418339Butyllithium2×

Product 1

HCID 21706484Ethyl 1-methyl-1-(4-methylphenyl)ethanesulfonateYield 77%

Conditions

Temperature
-40 °C

Procedure

To a solution of butyllithium (2.5M in hexanes, 2.94 mL) in THF (3.5 mL) cooled to -60 ° C. was added ethyl 4-methylphenylmethanesulfonate (1.05 g, 4.91 mmol) in THF (5 mL). After 15 minutes, iodomethane (0.61 mL, 9.8 mmol) was added, and the mixture was stirred for 1 hour at -50 to -30° C. The mixture was recooled to -60° C., and further butyllithium (2.94 mL) and iodomethane (0.61 mL) were added. The reaction was quenched with aqueous ammonium chloride, and extracted with ether. The organic phase was dried (K2CO3), filtered and evaporated. Chromatography of the residue over silica gel (15% ethyl acetate/hexane) gave ethyl 1-methyl-1-(4-methylphenyl)ethanesulfonate (0.917 g, 3.79 mmol, 77%).

Workup

  1. customwas recooled to -60° C.
  2. customThe reaction was quenched with aqueous ammonium chloride
  3. extractionextracted with ether
  4. dry with materialThe organic phase was dried (K2CO3)
  5. filtrationfiltered
  6. customevaporated

Sources & evidence

ORD record
ord-4b0a5edf078442258a460656800a0af3
Source dataset
uspto-grants-2000_04
Patent number
US06054470

Reaction notes

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