Réaction #2275726

ord-dd451fcaeae44a818125fabc4e674147

Équation de réaction

OC1CCC2(CC1)OCCO2
1,4-dioxa-spiro[4.5]decan-8-ol
Cc1ccc(S(=O)(=O)Cl)cc1
TsCl
Cc1ccc(S(=O)(=O)OC2CCC3(CC2)OCCO3)cc1
title compound
Cc1ccc(S(=O)(=O)OC2CCC3(CC2)OCCO3)cc1
Toluene-4-sulfonic acid 1,4-dioxa-spiro[4.5]dec-8-yl ester

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe solution was partitioned between DCM and water
  2. 2
    LavageThe organic layer was washed with brine
  3. 3
    Séchagedried over anhydrous Na2SO4
  4. 4
    Filtrationfiltered
  5. 5
    Concentrationconcentrated
  6. 6
    Autreto give white solid, which
  7. 7
    Autrewas then purified by silica gel column on a CombiFlash® system (Teledyne Isco, Inc, Lincoln, Neb.) system

Mode opératoire

A solution of 1,4-dioxa-spiro[4.5]decan-8-ol (prepared according to the procedure of Kayser, Margaret M.; Clouthier, Christopher M. Journal of Organic Chemistry (2006), 71(22), 8424-8430, 11 g, 70 mmol) in DCM (100 mL) was treated with TEA (11 mL, 77 mmol) followed by TsCl (Aldrich, 13.3 g, 70 mmol) slowly at 0° C. The reaction was warmed to room temperature over 2 hours. The solution was partitioned between DCM and water. The organic layer was washed with brine, dried over anhydrous Na2SO4, filtered and concentrated to give white solid, which was then purified by silica gel column on a CombiFlash® system (Teledyne Isco, Inc, Lincoln, Neb.) system using hexanes and ethyl acetate (from 10% ethyl acetate to 100% ethyl acetate) to afford the title compound as white solid.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08324186B2uspto-grants-2012_12