Reaktion #666574

ord-13fba2873f654242aa082e8919a1f6f3

Reaktionsgleichung

O
water
CC(C)(O)CCO
3-methylbutane-1,3-diol
Cc1ccc(S(=O)(=O)Cl)cc1
4-methylbenzenesulfonyl chloride
Cc1ccc(S(=O)(=O)OCCC(C)(C)O)cc1
title compound
Ausbeute 79.0%
Cc1ccc(S(=O)(=O)OCCC(C)(C)O)cc1
3-hydroxy-3-methylbutyl toluene-4-sulfonate
Ausbeute 79.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeto allow for layer separation
  2. 2
    WaschenThe obtained organic layer was washed successively with aqueous sulfuric acid and water (twice)
  3. 3
    SonstigeThe solvent in the obtained organic layer was evaporated
  4. 4
    Sonstigethe residue was azeotropically evaporated with toluene (500 ml)

Vorschrift

Under a nitrogen atmosphere, 3-methylbutane-1,3-diol (300 g) was dissolved in pyridine (900 ml), and a solution of 4-methylbenzenesulfonyl chloride (500 g) in toluene (900 ml) and acetonitrile (125 ml) was added dropwise over 2 hr. The reaction mixture was stirred at room temperature for 4 hr, and toluene (500 ml) and water (1800 ml) were added to allow for layer separation. The obtained organic layer was washed successively with aqueous sulfuric acid and water (twice). The solvent in the obtained organic layer was evaporated, and the residue was azeotropically evaporated with toluene (500 ml) to give the title compound (535 g).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09040717B2uspto-grants-2015_05