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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570128Generated: October 25, 2026

Triethylamine → 2,2-Difluoropropane-1,3-diyl dimethanesulfonate

https://huagongshe.com/reaction/570128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2,2-Difluoropropane-1,3-diolHCID 95744—
SolventDichloromethaneHCID 6344—
Product2,2-Difluoropropane-1,3-diyl dimethanesulfonateHCID 24287184%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 5 g (44.6 mmol) 2,2-difluoropropane-1,3-diol (prepared as described in J. Med. Chem. 1994, 37, 1857-1864) in DCM (50 mL) was added triethylamine (18.6 mL, 133.83 mmol) and methane sulphonyl chloride (6.9 mL, 89.22 mmol) at 0° C. and stirred for 1 h at 0° C. Thereafter the reaction mixture was quenched with water and extracted with DCM. The organic layer was dried over anhydrous sodium sulphate and concentrated to afford 2,2-difluoropropane-1,3-diyl dimethanesulfonate (9 g, 84%) which was used immediately in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023844B2
Source datasetuspto-grants-2015_05
ORD IDord-6897520d27f9497e907addb4497dad07
Source noteuspto-grants-2015_05