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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 253993생성일: 2026년 10월 24일

Dimethylformamide → 2-(N-(ethoxycarbonyl)-N-(2-(thiophen-2-yl)ethyl)amino)acetyl chloride

https://huagongshe.com/ko/reaction/253993

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Hypochlorous AcidHCID 24341—
반응물Oxalyl chlorideHCID 65578—
반응물[Ethoxycarbonyl-(2-thiophen-2-yl-ethyl)-amino]-acetic acidHCID 59302576—
용매DichloromethaneHCID 6344—
생성물2-(N-(ethoxycarbonyl)-N-(2-(thiophen-2-yl)ethyl)amino)acetyl chlorideHCID 86616061—

반응 단계

2-(N-(Ethoxycarbonyl)-N-(2-(thiophen-2-yl)ethyl)amino)acetic acid (14 g, 54.41 mmol) was dissolved in dry dichloromethane (DCM) (300 mL). To this suspension was added 0.1 mL of DMF, followed by the careful addition of oxyl chloride (10.4 g, 81.93 mmol). The reaction mixture was stirred at room temperature for 1 hour, at which time 0.5 mL of additional oxalyl chloride was added. The solvent was evaporated under vacuum to give 2-(N-(ethoxycarbonyl)-N-(2-(thiophen-2-yl)ethyl)amino)acetyl chloride. This acid chloride was re-dissolved in dry DCM (300 mL) and AlCl3 (18.1 g, 135.74 mmol) was added at room temperature. The reaction was kept at room temperature for 1 hour then quenched by the slow addition of ethanol (about 10 mL). The mixture was then poured into ice and stirred for 1 hr. The aqueous mixture was extracted with DCM (3×150 mL). The combined organic layers were dried over MgSO4, filtered, and evaporated to give a residue, which was purified by silica gel chromatography to produce ethyl 4,5,7,8-tetrahydro-4-oxothieno[3,2-d]azepine-6-carboxylate (7.4 g, 30.92 mmol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07872031B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-a31c73bac5bb40fa9162c0ae8a1a1bb6
출처 메모uspto-grants-2011_01