Reaction #2275726

ord-dd451fcaeae44a818125fabc4e674147

Reaction equation

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

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

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

Procedure

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.v1Patent: US08324186B2uspto-grants-2012_12