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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1830558생성일: 2026년 10월 26일

Dimethylformamide → 2-(1,3-Dioxolan-2-yl)-3-furaldehyde

https://huagongshe.com/reaction/1830558

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Oxalic acid dihydrateHCID 61373—
반응물2-(3-Bromofuran-2-yl)-1,3-dioxolaneHCID 12372309—
반응물HCID 178418306HCID 178418306—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물2-(1,3-Dioxolan-2-yl)-3-furaldehydeHCID 2204762268%

반응 조건

온도-78 °C

반응 단계

2-(3-Bromo-2-furyl)-1,3-dioxolane (438 mg, 2.0 mmol) is dissolved in Et2O (5 mL) in an oven-dried flask, under nitrogen, cooled to −78° C., treated dropwise with tert-butyllithium (2.59 mL, 4.4 mmol) and stirred for 1 h. DMF (178 μL, 2.3 mmol) in Et2O (2 mL) is added dropwise, the mixture stirred for 4 h at −78° C., then treated with oxalic acid dihydrate (504 mg, 4.0 mmol) followed by water (2 mL). The cooling bath is removed and the mixture allowed to warm to rt over 1 h. The mixture is diluted with water (20 mL) and EtOAc (20 mL), the layers are separated and the aqueous layer extracted with EtOAc (1×20 mL). The organics are dried over Na2SO4 and concentrated to a yellow oil. The crude material is chromatographed over 12 g slurry-packed silica gel, eluting with 15% EtOAc/hexane. The appropriate fractions are combined and concentrated in vacuo to afford 228 mg (68%) of 2-(1,3-dioxolan-2-yl)-3-furaldehyde as a pale yellow oil. MS (EI) m/z: 168 (M+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07067515B2
출처 데이터셋uspto-grants-2006_06
ORD IDord-a31de2cd9c224a8b8c1344c5513eb6ae
출처 메모uspto-grants-2006_06