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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 42748생성일: 2026년 10월 25일

Nitrogen → 2-(5-Chloromethyl-furan-2-yl)-2-methyl-[1,3]dioxolane

https://huagongshe.com/reaction/42748

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물DichloromethaneHCID 6344—
반응물TriethylamineHCID 8471—
반응물[5-(2-Methyl-[1,3]dioxolan-2-yl)-furan-2-yl]-methanolHCID 66929165—
촉매4-(Dimethylamino)pyridineHCID 14284—
생성물2-(5-Chloromethyl-furan-2-yl)-2-methyl-[1,3]dioxolaneHCID 66928965—

반응 단계

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of [5-(2-methyl-[1,3]dioxolan-2-yl)-furan-2-yl]-methanol (3.50 g, 19.00 mmol) in dry CH2Cl2 (35.0 mL) was treated at 0° C. with Et3N (3.44 mL, 22.80 mmol) followed by DMAP (232 mg, 1.90 mmol) and Ms-C1 (1.77 mL, 22.80 mmol). After stirring at rt for 2 h, the reaction mixture was quenched with water (40 mL), extracted with CH2Cl2 (40 mL) and the combined org. extracts were dried over MgSO4, filtered, and the solvents were removed under reduced. Purification of the residue by FC (8:2:0.1 hept-EA-Et3N) gave the title compound as a yellow oil: TLC:rf (4:1 hept-EA)=0.35.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536209B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-2dc9582667fa4ebe80cf6a43d935acf4
출처 메모uspto-grants-2013_09