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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1592382생성일: 2026년 10월 25일

1,2-Dimethoxyethane → 3-Thiophen-2-yl-pyridine-2-carbaldehyde

https://huagongshe.com/reaction/1592382

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DimethoxyethaneHCID 8071—
반응물Sodium CarbonateHCID 10340—
반응물2-Thiopheneboronic acidHCID 2733960—
반응물3-Bromopyridine-2-carbaldehydeHCID 16414231—
촉매HCID 178418397HCID 178418397—
용매TetrahydrofuranHCID 8028—
생성물3-Thiophen-2-yl-pyridine-2-carbaldehydeHCID 8659475163.4%

반응 조건

온도90 °C

반응 단계

A stirred solution of 3-bromo-pyridine-2-carbaldehyde (126 mg, 0.675 mmol) and 2-thiopheneboronic acid (91.6 mg, 0.716 mmol) in a mixture of THF (0.75 mL), DME (2.0 mL) and 2M Na2CO3 (0.75 mL) was degassed with Ar for 15 minutes, after which Pd(PPh3)4 (39 mg, 0.034 mmol) was added and the heterogeneous mixture heated to 90° C. for 4 h. The reaction was quenched with brine (15 mL) and diluted with EtOAc (40 mL). The organic layer was separated, washed with brine (2×15 mL), dried (Na2SO4), filtered and concentrated in vacuo. Purification by flash chromatography on silica gel (Hexanes/EtOAc, 80:20) gave 3-thiophen-2-yl-pyridine-2-carbaldehyde (81 mg, 63%) as a yellow oil. 1H NMR (CDCl3) δ 7.13-7.22 (m, 2H), 7.48-7.57 (m, 2H), 7.92 (dd, 1H, J=7.9, 1.9 Hz), 8.82 (dd, 1H, J=6.0, 1.5 Hz), 10.23 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07291631B2
출처 데이터셋uspto-grants-2007_11
ORD IDord-29d66fd3cccf46a2ae771859362f89a9
출처 메모uspto-grants-2007_11