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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 253100생성일: 2026년 10월 26일

Iodine → Ethyl 5-benzylnicotinate

https://huagongshe.com/reaction/253100

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물Benzyl BromideHCID 7498—
반응물Ethyl 5-bromopyridine-3-carboxylateHCID 140785—
반응물Sodium BicarbonateHCID 516892—
촉매ZincHCID 23994—
용매BenzeneHCID 241—
용매Ethyl AcetateHCID 8857—
용매DimethylacetamideHCID 31374—
생성물Ethyl 5-benzylnicotinateHCID 66610002—

반응 조건

온도80 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07872009B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-50cc732d3b0e420b88462e0f014fffc4
출처 메모uspto-grants-2011_01