Solketal → (2,2-Dimethyl-1,3-dioxolan-4-yl)methyl methanesulfonate

HRID 246044

Reaction equation

HRID 246044 reaction equation
[CH3:1][C:2]1([CH3:9])[O:6][CH:5]([CH2:7][OH:8])[CH2:4][O:3]1.C(N(CC)CC)C.[CH3:17][S:18](Cl)(=[O:20])=[O:19]>ClCCl>[CH3:1][C:2]1([CH3:9])[O:6][CH:5]([CH2:7][O:8][S:18]([CH3:17])(=[O:20])=[O:19])[CH2:4][O:3]1

Participants

5

Conditions

Temperature
0 °C

Procedure

To a solution of (2,2-dimethyl-[1,3]dioxolan-4-yl)-methanol (1.25 g, 9.46 mmol) and triethylamine (9.2 ml, 66.2 mmol) in dichloromethane (60 ml) at 0° C. was slowly added methanesulfonyl chloride (2.2 ml, 28.4 mmol). The reaction mixture was stirred at 0° C. for 2 h then quenched with water and the aqueous layer was extracted with dichloromethane. The combined organics were washed with 10% citric acid, sat NaHCO3, and brine then dried over MgSO4 and concentrated to afford methanesulfonic acid 2,2-dimethyl-[1,3]dioxolan-4-ylmethyl ester as a light brown oil which was used without further purification.

Workup

  1. customat 0° C.
  2. customthen quenched with water
  3. extractionthe aqueous layer was extracted with dichloromethane
  4. washThe combined organics were washed with 10% citric acid
  5. dry with materialthen dried over MgSO4
  6. concentrationconcentrated

Sources & evidence

ORD record
ord-402d486a81b84fbaa9544902b15926cb
Source dataset
uspto-grants-2014_02
Patent number
US08658646B2

Linked notes

Loading…