p-Toluenesulfonic acid monohydrate → p-Toluenesulfonic acid

HRID 325576Notes

Reaction equation

HRID 325576 reaction equation
O.[C:2]1([CH3:12])[CH:7]=[CH:6][C:5]([S:8]([OH:11])(=[O:10])=[O:9])=[CH:4][CH:3]=1>O1CCOCC1>[CH3:12][C:2]1[CH:7]=[CH:6][C:5]([S:8]([OH:11])(=[O:10])=[O:9])=[CH:4][CH:3]=1

Participants

3

Procedure

p-Nitrobenzyl bromide (21.6 g, 100 mmol) and the salt G (25.5 g, 100 mmol) were dissolved in anhydrous dimethylformamide (100 ml), and the solution was stirred at room temperature for 24 hours. The reaction mixture was then diluted with ethyl acetate (300 ml), washed with saturated NaHCO3, brine, dried (Na2SO4), and concentrated in vacuo to yield ester H as a viscous oil (36.5 g). This material, quite pure as determined by TLC, was then dissolved in 1,4-dioxane (80 ml) to which was added p-toluenesulfonic acid monohydrate (19.02 g, 100 mmol). After stirring at room temperature for 20 hours, the product precipitated from solution, was filtered, washed with ether, and dried to yield the p-toluenesulfonate salt (36.04 g, 84.0% from G) as a white, fluffy, solid, mp 142°-3°.

Workup

  1. customthe product precipitated from solution
  2. filtrationwas filtered
  3. washwashed with ether
  4. customdried

Sources & evidence

ORD record
ord-5143cc5ec6fa4a9295939d21242b8705
Source dataset
uspto-grants-1984_04
Patent number
US04440682

Reaction notes

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