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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 323665생성일: 2026년 10월 24일

Triethylamine → 3,5-Dichloro-1-(3,3-dichloro-2-propenyloxy)-4-(3-(5-bromo-2-furancarboxamido)propyloxy)-benzene

https://huagongshe.com/ko/reaction/323665

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물5-Bromo-2-furanecarboxylic acidHCID 68511—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물3-[2,6-Dichloro-4-(3,3-dichloro-allyloxy)-phenoxy]-propylamineHCID 15869744—
용매ChloroformHCID 6212—
용매Ethyl AcetateHCID 8857—
생성물3,5-Dichloro-1-(3,3-dichloro-2-propenyloxy)-4-(3-(5-bromo-2-furancarboxamido)propyloxy)-benzeneHCID 2200677167.9%

반응 단계

To a mixture of 0.35 g of 4-(3-aminopropyloxy)-3,5-dichloro-1-(3,3-dichloro-2-propenyloxy)benzene, 0.19 g of 5-bromo-2-furancarboxylic acid, 0.18 ml of triethylamine and 10 ml of chloroform was added 0.23 g of WSC hydrochloride, while stirring at room temperature. After stirring at room temperature for 6 hours, the reaction mixture was concentrated to give a residue. The residue was dissolved in 50 ml of ethyl acetate, and the ethyl acetate layer was successively washed with 10% hydrochloric acid, saturated aqueous sodium hydrogen carbonate solution and saturated saline solution, dried over anhydrous magnesium sulfate, and then concentrated to give a residue. The residue was subjected to silica gel chromatography, which afforded 0.35 g of 3,5-dichloro-1-(3,3-dichloro-2-propenyloxy)-4-(3-(5-bromo-2-furancarboxamido)propyloxy)-benzene (64% yield), nD24.0 1.5918.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06214835B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-df8d480037dd4f35ac09d619c4db673b
출처 메모uspto-grants-2001_04