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HRID 37993作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/37993

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物WaterHCID 962—
反応物SolketalHCID 7528—
反応物Oxalyl chlorideHCID 65578—
溶媒DichloromethaneHCID 6344—
生成物2,2-Dimethyl-1,3-dioxolane-4-carboxaldehydeHCID 110702—

反応条件

温度-60 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524702B2
出典データセットuspto-grants-2013_09
ORD IDord-0ecb885addee473b936a27c496770b68
出典メモuspto-grants-2013_09