Reaktion #165701

ord-7a7fd07a31984e249677bcd4f6de1b19

Reaktionsgleichung

CC(C)(O)CCO
3-methylbutane-1,3-diol
Cc1ccc(S(=O)(=O)Cl)cc1
para-toluenesulfonyl chloride
O
H2O
Cc1ccc(S(=O)(=O)OCCC(C)(C)O)cc1
title compound
Cc1ccc(S(=O)(=O)OCCC(C)(C)O)cc1
3-hydroxy-3-methylbutyl 4-methylbenzenesulfonate

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionthe mixture was extracted with ethyl acetate (2×50 mL)
  2. 2
    WaschenThe combined organics were washed with H2O (2×50 mL)
  3. 3
    Trocknendried over MgSO4
  4. 4
    Filtrationfiltered
  5. 5
    Einengenconcentrated under reduced pressure
  6. 6
    Sonstigedried under vacuum (˜1 mm Hg)

Vorschrift

To a solution of 3-methylbutane-1,3-diol (2.13 mL, 20 mmol) in pyridine (20 mL) at 0° C. was added para-toluenesulfonyl chloride (3.8 g, 20 mmol) in pyridine (10 mL) drop-wise over 15 minutes. This mixture stirred at ambient temperature for 3 hours and 35 mL H2O was added and the mixture was extracted with ethyl acetate (2×50 mL). The combined organics were washed with H2O (2×50 mL), dried over MgSO4, filtered, concentrated under reduced pressure and dried under vacuum (˜1 mm Hg) to afford the title compound. MS (ESI) m/z 276 (M+18)+.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08841334B2uspto-grants-2014_09