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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1860269생성일: 2026년 10월 25일

Ethyl chloroacetate → Ethyl-5-[(hydroxyimino)methyl]-2-nitro-3-thiopheneacetate

https://huagongshe.com/reaction/1860269

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl chloroacetateHCID 7751—
반응물5-Nitro-2-thiophenecarboxaldehyde oximeHCID 350516—
반응물Potassium tert-butoxideHCID 23665647—
용매DimethylformamideHCID 6228—
생성물Ethyl-5-[(hydroxyimino)methyl]-2-nitro-3-thiopheneacetateHCID 8580189627.1%

반응 조건

온도-30 °C

반응 단계

Potassium tertiary-butoxide (960 mg, 8.6 mmol) was dissolved in N,N-dimethylformamide (10 ml) and the solution cooled to −30° C. A solution of 5-nitro-2-thiophenecarboxaldehyde oxime (400 mg, 2.86 mmol) and ethyl chloroacetate (356 mg, 2.86 mmol) was added dropwise in dry N,N-dimethylformamide (5 ml) over 5 minutes. The reaction mixture was stirred at −30° C. for 30 minutes then quenched with 2M HCl (50 ml), diluted with ethyl acetate, washed with water, dried over magnesium sulfate and evaporated to dryness. The residue was chromatographed on silica gel using hexane/diethyl ether (1:2) as eluent to give 200 mg of ethyl-5-[(hydroxyimino)methyl]-2-nitro-3-thiopheneacetate as a tan solid. MS(ES): m/e 227 [M+H].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06528653B2
출처 데이터셋uspto-grants-2003_03
ORD IDord-3725d1bfa4d54d478308ee4da6cc06a7
출처 메모uspto-grants-2003_03