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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 459910생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/459910

반응식

참여 물질

역할이름HCID투입량
반응물Oxalyl chlorideHCID 65578—
반응물2-Furylglyoxylic acidHCID 73846—
반응물3-Quinuclidinol, (-)-HCID 91404—
촉매DimethylformamideHCID 6228—
용매ChloroformHCID 6212—
생성물2-fur-2-yl-2-oxoacetic acid (3R)-1-azabicyclo[2.2.2]oct-3-yl esterHCID 6659205352.8%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07196098B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-05ca160b85614b93b19c52d97f4c614c
출처 메모uspto-grants-2007_03