Pyridine → Methyl 3-(p-tolylsulfonyloxy)-2,2-dimethylpropanoate

HRID 2182902Notes

Reaction equation

HRID 2182902 reaction equation
[CH3:1][C:2]([CH3:9])([CH2:7][OH:8])[C:3]([O:5][CH3:6])=[O:4].[C:10]1([CH3:20])[CH:15]=[CH:14][C:13]([S:16](Cl)(=[O:18])=[O:17])=[CH:12][CH:11]=1.N1C=CC=CC=1>CN(C)C1C=CN=CC=1.C1(C)C=CC=CC=1>[CH3:1][C:2]([CH3:9])([CH2:7][O:8][S:16]([C:13]1[CH:14]=[CH:15][C:10]([CH3:20])=[CH:11][CH:12]=1)(=[O:18])=[O:17])[C:3]([O:5][CH3:6])=[O:4]

Participants

6

Reactant 3

HCID 1049PyridineHCID 73974-Toluenesulfonyl chlorideHCID 84152Methyl 3-hydroxypivalate

Product 1

HCID 22479327Methyl 3-(p-tolylsulfonyloxy)-2,2-dimethylpropanoateYield 108%

Reagents, catalysts & solvents 2

HCID 142844-(Dimethylamino)pyridineCatalystHCID 1140TolueneSolvent

Procedure

A mixture of methyl 2,2-dimethyl-3-hydroxypropionate (100 g, 0.76 mol), 4-toluenesulfonyl chloride (151 g, 0.80 mol), 4-dimethylaminopyridine (4.6 g, 0.038 mol), and pyridine (200 mL) was stirred for 20 hrs and then was diluted with 200 mL toluene, stirred for 30 min, and filtered. The filtrate was concentrated to 250 mL under reduced pressure, diluted with 100 mL toluene, filtered, and concentrated. The residue was suspended in 200 mL hexanes, and the solvent was removed under reduced pressure to yield the title compound, desired product (235 g, 100%) contaminated by a trace of 4-toluenesulfonyl chloride.

Workup

  1. stirringstirred for 30 min
  2. filtrationfiltered
  3. concentrationThe filtrate was concentrated to 250 mL under reduced pressure
  4. additiondiluted with 100 mL toluene
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customthe solvent was removed under reduced pressure

Sources & evidence

ORD record
ord-95a3d97088754a1db8825dfb2f406b1d
Source dataset
uspto-grants-2005_05
Patent number
US06897227B2

Reaction notes

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