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HRID 459910作成日:2026年10月26日

Oxalyl chloride → 2-fur-2-yl-2-oxoacetic acid (3R)-1-azabicyclo[2.2.2]oct-3-yl ester

https://huagongshe.com/reaction/459910

反応式

関与物質

役割名称HCID仕込み量
反応物Oxalyl chlorideHCID 65578—
反応物2-Furylglyoxylic acidHCID 73846—
反応物3-Quinuclidinol, (-)-HCID 91404—
触媒DimethylformamideHCID 6228—
溶媒ChloroformHCID 6212—
生成物2-fur-2-yl-2-oxoacetic acid (3R)-1-azabicyclo[2.2.2]oct-3-yl esterHCID 6659205352.8%

反応手順

Oxalyl chloride (9.75 ml, 0.112 mol) was added to a solution of oxofuran-2-ylacetic acid (10 g, 0.071 mol) and dimethylformamide (one drop) in 150 ml of chloroform (etanol free) at 01 C. The mixture was stirred and allowed to warm at room temperature. After five hours the solvent was evaporated. The residue was dissolved in chloroform and evaporated again. This procedure was repeated two times. The product obtained was disolved in CHCl3 (150 ml) and a solution of 3(R)-quinuclidinol (10.90 g, 0.086 mol) in CHCl3 (150 ml) was added to this at 01 C. The mixture was stirred and allowed to warm at room temperature. After 15 h at r.t., the mixture was washed with 10% aqueous potassium carbonate, then with water, dried over Na2SO4 and evaporated to give 9.34 g (52.5%) of the title compound as a dark oil. Estructure confirmed by NMR.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07196098B2
出典データセットuspto-grants-2007_03
ORD IDord-05ca160b85614b93b19c52d97f4c614c
出典メモuspto-grants-2007_03