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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 483363생성일: 2026년 10월 24일

Sodium Iodide → Noradenalone hydrochloride

https://huagongshe.com/ko/reaction/483363

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물Sodium AzideHCID 33557—
반응물2-Chloro-3',4'-dihydroxyacetophenoneHCID 66834—
용매AcetoneHCID 180—
생성물Noradenalone hydrochlorideHCID 19983150.4%

반응 조건

온도40 °C

반응 단계

10 g (53.6 mmol) of 2-chloro-3',4'-dihydroxyacetophenone was dissolved in 50 ml of acetone, and 600 mg (4.0 mmol) of sodium iodide and 5.23 g (80.5 mmol) of sodium azide were added thereto. The mixture was refluxed for 24 hours. The insolubles in the reaction solution were removed by filtration, and the filtrate was concentrated under reduced pressure. To the reaction solution, ethyl acetate was added, and the mixture was washed sequentially with water and with a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the oily residue was dissolved in 100 ml of methanol and 13.6 ml of concentrated hydrochloric acid. 1.5 g of 10% palladium carbon catalyst was added to the solution, and the mixture was stirred under heating at 40° C. under a hydrogen gas stream for 5 hours. The reaction solution was filtered, and the filtrate was concentrated under reduced pressure. To the concentrated residue, acetone was added, and the precipitated crystals were collected by filtration to obtain 5.5 g (yield: 50.4%) of 2-amino-3',4'-dihydroxyacetophenone hydrochloride.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05225406
출처 데이터셋uspto-grants-1993_07
ORD IDord-c4f7e57300d342bfa4d5e6d412840967
출처 메모uspto-grants-1993_07