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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 507262생성일: 2026년 10월 25일

Diethyl Ether → ethyl [(1-benzyl-1H-benzimidazol-2-yl)sulfanyl]acetate

https://huagongshe.com/reaction/507262

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참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물Benzyl BromideHCID 7498—
반응물ethyl 2-(1H-1,3-benzodiazol-2-ylsulfanyl)acetateHCID 21564—
반응물Sodium hydrideHCID 24758—
용매DimethylformamideHCID 6228—
생성물ethyl [(1-benzyl-1H-benzimidazol-2-yl)sulfanyl]acetateHCID 97543131%

반응 조건

온도0 °C

반응 단계

To a stirred solution of ethyl 2-(1H-benzo[d]imidazol-2-ylthio)acetate 4a (11.2 g, 47.6 mmol, 1.0 eq.) in 10:1 diethyl ether:dimethylformamide (450 mL) at 0° C., was added 60% sodium hydride in mineral oil (2.09 g, 52.3 mmol, 1.1 eq.), and the reaction was stirred at 0° C. for 20 minutes. Benzyl bromide (9.78 g, 57.1 mmol, 1.2 eq.) was added at 0° C., and the reaction was stirred with warming to room temperature for 16 hours. The reaction mixture was quenched with methanol (100 mL) and concentrated in vacuo. The residue was taken into hot chloroform (400 mL) and filtered. The filtrate was washed with water (200 mL), 1M HCl (200 mL) and brine (200 mL). The organic layer was dried over magnesium sulfate and concentrated in vacuo. Purification by flash chromatography (10% EtOAc:90% petroleum ether) gave 4b as a pale-yellow solid (4.82 g, 30%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07786139B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-39bea83ebfac46b2b16214d7f5e1304e
출처 메모uspto-grants-2010_08