Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593434Generated: October 25, 2026

Dimethyl Sulfoxide → 2,2-Dimethyl-1,3-dioxolane-4-carboxaldehyde

https://huagongshe.com/reaction/593434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantWaterHCID 962—
ReactantSolketalHCID 7528—
ReactantOxalyl chlorideHCID 65578—
SolventDichloromethaneHCID 6344—
Product2,2-Dimethyl-1,3-dioxolane-4-carboxaldehydeHCID 110702—

Reaction Conditions

Temperature-60 °C

Reaction Steps

A solution of anhydrous DMSO (3.41 mL, 48 mmol) in CH2Cl2 (5 mL) was added dropwise to a stirred solution of oxalyl chloride (1.92 mL, 22 mmol) in CH2Cl2 (50 mL) at −60° C. To this mixture was added a solution of (2,2-dimethyl-[1,3]dioxolan-4-yl)-methanol (2.48 mL, 20 mmol) in CH2Cl2 (10 mL). The resulting mixture was stirred for 15 min at −60° C. TEA (13.9 mL, 100 mmol) was added dropwise. The reaction mixture was then warmed to room temperature. Water (50 mL) and CH2Cl2 (50 mL) were added. The organic layer was separated and washed with water (25 mL). The aqueous layer was extracted with CH2Cl2 (3×50 mL). The organic layers were dried over MgSO4, filtered, and concentrated under reduced pressure to afford the crude 2,2-dimethyl-1,3-dioxolane-4-carbaldehyde that was used directly without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242964B2
Source datasetuspto-grants-2016_01
ORD IDord-cb8ab75ac5b34eb38eb55a4c4112ef1c
Source noteuspto-grants-2016_01