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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 324140생성일: 2026년 10월 25일

1,2-Dichloroethane → N-(8-Phenyloctyl)-3-iodo-4-hydroxybenzamide

https://huagongshe.com/reaction/324140

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물DiisopropylethylamineHCID 81531—
반응물8-Phenyloctan-1-amineHCID 145556—
반응물4-Hydroxy-3-iodobenzoic acid (2IPCOOH)HCID 449473—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물N-(8-Phenyloctyl)-3-iodo-4-hydroxybenzamideHCID 2223756499%

반응 단계

To a stirring solution of 3-iodo-4-hydroxy-benzoic acid (2.64 g, 10.00 mmol) in fresh DMF (5 mL) at ambient temperature under an atmosphere of N2 was added EDC (2.11 g, 11.00 mmol), HOBt (1.49 g, 11.00 mmol) and DIPEA (1.94 g, 2.60 mL, 15.00 mmol). The solution was allowed to stir at ambient temperature for 1 hour at which time 8-phenyl-octylamine (2.46 g, 2.39 mL, 12 mmol) was added at one time. The solution was allowed to stir for an additional 4 hours at which time the it was diluted with water (250 mL) and extracted with ethyl acetate (250 mL). The organic phase was washed with water (2×250 mL), saturated aqueous NaHCO3 (250 mL) and saturated aqueous NaCl (250 mL). The solvent was removed in vacuo to yield 4.62 g of crude oil. The crude oil was purified by column chromatography (7:3 hexane:ethyl acetate) to yield 4.47 g (99%) of the desired product as a clear oil, which crystallized upon standing. 1H NMR (CDCl3)6 8.19 (dd, 2H), 7.60 (dd, 1H), 7.20 (m, 4H), 6.97 (dd, 1H), 6.32 (t, 1H), 3.39 (q, 2H), 2.57 (t, 2H), 1.58 (m, 4H), 1.30 (m, 8H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06214877B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-594339c45f9542dea6629453f10e9d53
출처 메모uspto-grants-2001_04