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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2267957생성일: 2026년 10월 26일

Sodium Iodide → HCID 18348169, 화합물

https://huagongshe.com/reaction/2267957

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물1-Piperazinecarboxylic acid, ethyl esterHCID 8431—
반응물TriethylamineHCID 8471—
반응물(2-Chlorophenyl)(4-chlorophenyl)methyl chlorideHCID 247330—
용매TolueneHCID 1140—
용매DichloromethaneHCID 6344—
용매HexaneHCID 8058—
생성물HCID 18348169HCID 1834816928.3%

반응 단계

A stirred solution of 2.5 grams (0.009 mole) of (2-chlorophenyl)(4-chlorophenyl)methyl chloride, 1.6 grams (0.010 mole) of ethyl 1-piperazine-carboxylate, 1.4 mL (0.010 mole) of triethylamine, and 1.2 grams (0.008 mole) of sodium iodide in 25 mL of toluene was heated at reflux for about 18 hours. The resulting precipitate was collected by filtration. The filtrate was cooled to ambient temperature and 200 mL of aqueous saturated sodium bicarbonate solution was added to it. The mixture was extracted with two 100 mL portions of ethyl acetate. The combined ethyl acetate layers were washed with two 25 mL portions of an aqueous saturated sodium chloride solution. The organic layer was dried with sodium sulfate and concentrated under reduced pressure, yielding 3.2 grams of crude material. The crude material was subjected to column chromatography on silica gel with 50-25% hexane in methylene chloride, followed by pure methylene chloride, as eluants. The product-containing fractions were combined and concentrated under reduced pressure, yielding 1.0 gram of N-(ethoxycarbonyl)-N′-[(2-chlorophenyl)(4-chlorophenyl)methyl]piperazine. The NMR spectrum was consistent with the proposed structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USH0002007H1
출처 데이터셋uspto-grants-2001_12
ORD IDord-893a87e3b3c946a0b94bbe980dee7c6a
출처 메모uspto-grants-2001_12