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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 42761생성일: 2026년 10월 26일

Nitrogen → 2-[3-(2-Methyl-[1,3]dioxolan-2-yl)-benzyl]-4-nitro-2H-[1,2,3]triazole

https://huagongshe.com/reaction/42761

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물DiisopropylethylamineHCID 81531—
반응물4-nitro-2H-1,2,3-triazoleHCID 278150—
반응물(3-(2-Methyl-[1,3]dioxolan-2-yl)-phenyl)methyl methanesulfonateHCID 86649478—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물2-[3-(2-Methyl-[1,3]dioxolan-2-yl)-benzyl]-4-nitro-2H-[1,2,3]triazoleHCID 67365422—

반응 조건

온도50 °C

반응 단계

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 4-nitro-2H-[1,2,3]triazole (50 mg, 0.43 mmol) in DMF (1.0 mL) was treated with DIPEA (0.15 mL, 0.87 mmol). After 30 min, a solution of methanesulfonic acid 3-(2-methyl-[1,3]dioxolan-2-yl)-benzyl ester (106 mg, 0.52 mmol) in DMF (1.0 mL) was added and the reaction mixture was stirred for 3 days at 50° C. Water (10 mL), followed by EA (10 mL) were added. The aq. layer was extracted with EA (10 mL) and the combined org. extracts were dried over Na2SO4, filtered, and the solvents were removed under reduced pressure. Purification of the residue by FC (2:1 hept-EA) gave the title compound as a colorless oil: TLC:rf (1:2 hept-EA)=0.42. LC-MS-conditions 02: tR=0.99 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536209B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-5165ea9072ce49c6af505bbc9bc310b2
출처 메모uspto-grants-2013_09