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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 634370생성일: 2026년 10월 25일

Toluene → 4-(5-(3-(dimethylamino)prop-1-en-1-yl)thiophen-2-yl)-3-(1-hydroxyethyl)-1H-isochromen-1-one

https://huagongshe.com/reaction/634370

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물Ammonium ChlorideHCID 25517—
반응물(2-(Dimethylamino)ethyl)triphenylphosphonium bromideHCID 2724136—
반응물Potassium bis(trimethylsilyl)amideHCID 3251421—
반응물HCID 118131138HCID 118131138—
용매Ethyl AcetateHCID 8857—
용매1,4-DioxaneHCID 31275—
생성물4-(5-(3-(dimethylamino)prop-1-en-1-yl)thiophen-2-yl)-3-(1-hydroxyethyl)-1H-isochromen-1-oneHCID 12373564340,858.102%

반응 단계

In a 100 ml 3-necked round bottomed flask (2-(dimethylamino)ethyl)-triphenylphosphonium bromide (1569 mg, 3.79 mmol) was loaded and suspended under Argon in 15 ml of Dioxane. Potassium bis(trimethylsilyl)amide solution 0.5 M in toluene (6.0 ml, 3.03 mmol) was added drop wise and a yellow\orange color appeared. The mixture was further stirred for 20 min then 5-(3-(1-hydroxyethyl)-1-oxo-1H-isochromen-4-yl)thiophene-2-carbaldehyde (Intermediate B37, 455 mg, 1.515 mmol) dissolved in 5 ml of dioxane was added The mixture was further stirred at rt for 2 h then poured into 100 ml of NH4Cl sat. sol. and 200 ml of EtOAc. Phases were separated and the organic one was dried over sodium sulfate. Solvents were removed and the crude was purified by chromatography eluting with DCM\20% MeOH in DCM mixtures to leave 4-(5-(3-(dimethylamino)prop-1-en-1-yl)thiophen-2-yl)-3-(1-hydroxyethyl)-1H-isochromen-1-one (220 mg, 0,619 mmol, 40.9% yield) as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09321776B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-c0c148c6293e483e94d77d900dc22546
출처 메모uspto-grants-2016_04