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HRID 253100作成日:2026年10月26日

Iodine → Ethyl 5-benzylnicotinate

https://huagongshe.com/reaction/253100

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物Benzyl BromideHCID 7498—
反応物Ethyl 5-bromopyridine-3-carboxylateHCID 140785—
反応物Sodium BicarbonateHCID 516892—
触媒ZincHCID 23994—
溶媒BenzeneHCID 241—
溶媒Ethyl AcetateHCID 8857—
溶媒DimethylacetamideHCID 31374—
生成物Ethyl 5-benzylnicotinateHCID 66610002—

反応条件

温度80 °C

反応手順

A suspension of Zn (1.0 g, 15 mmol) and I2 (130 mg, 0.5 mmol) in DMA (15 mL) was stirred vigorously until the red color dissipated (3-5 min). Benzyl bromide (1.7 g, 10 mmol) was introduced and the resulting slurry was heated at 80° C. for 2.5 h at which point Cl2Pd(PPh3)2 (250 mg, 0.35 mmol) and a solution of ethyl-5-bromonicotinate (1.1 g, 5.0 mmol) in benzene (10 mL) were introduced and the reaction was heated at 80° C. for 1 h. The reaction was allowed to cool to room temperature and was diluted with EtOAc (100 mL). The mixture was poured into NaHCO3 (5% aqueous, 100 mL). The layers were separated and the aqueous layer was extracted with EtOAc (2×50 mL). The combined organic layers were sequentially washed with H2O (3×100 mL) and brine before being dried over Na2SO4. Concentration and purification by silica gel chromatography (hexane→50% EtOAc/hexane) provided the title compound as a brown oil. MS m/z: 242.1 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07872009B2
出典データセットuspto-grants-2011_01
ORD IDord-50cc732d3b0e420b88462e0f014fffc4
出典メモuspto-grants-2011_01