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HRID 42763作成日:2026年10月25日

Nitrogen → 6-(4-Nitro-[1,2,3]triazol-2-yl)-hexan-2-one

https://huagongshe.com/reaction/42763

反応式

関与物質

役割名称HCID仕込み量
反応物NitrogenHCID 947—
反応物6-Bromohexan-2-oneHCID 25061—
反応物DiisopropylethylamineHCID 81531—
反応物4-nitro-2H-1,2,3-triazoleHCID 278150—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物6-(4-Nitro-[1,2,3]triazol-2-yl)-hexan-2-oneHCID 67365263—

反応条件

温度50 °C

反応手順

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a suspension of 4-nitro-2H-[1,2,3]triazole (114 mg, 1.00 mmol) in DMF (1.0 mL) was treated with DIPEA (0.34 mL, 2.00 mmol). After 30 min, a solution of 6-bromo-hexan-2-one (179 mg, 1.00 mmol) in DMF (1.0 mL) was added and the reaction mixture was stirred for 24 h 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 yellow oil: TLC:rf (2:1 hept-EA)=0.26. LC-MS-conditions 02: tR=0.86 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536209B2
出典データセットuspto-grants-2013_09
ORD IDord-5e25961a1c2a4638ac66cb199ce37e90
出典メモuspto-grants-2013_09