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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 840045생성일: 2026년 10월 25일

Propanoic acid, 3-iodo- → n-(2-Carboxyethyl)-2,3,3-trimethylindolinium iodide

https://huagongshe.com/reaction/840045

반응식

참여 물질

역할이름HCID투입량
반응물Propanoic acid, 3-iodo-HCID 8856—
반응물3H-Indole, 2,3,3-trimethyl-HCID 15427—
생성물n-(2-Carboxyethyl)-2,3,3-trimethylindolinium iodideHCID 18764709—

반응 조건

온도80 °C

반응 단계

A 2-necked 50 milliliter round-bottomed flask equipped with a magnetic stirring bar and an argon inlet was charged with re-distilled (pressure 2 mm Hg, temperature 45° C.) 2,3,3-trimethylindolenine (7.95 grams, 50.0 mmol) and 3-iodopropionic acid (2.00 grams, 10 mmol). The mixture was heated to 80° C. for 12 hours, during which time the product precipitated out of solution and formed a highly viscous medium. Upon cooling, the reaction mixture was extracted three times with 200 milliliter portions of diethyl ether to remove all of the unreacted starting material. The remaining crystalline solid was then dissolved in 10 milliliters of water, extracted three times with 50 milliliter portions of diethyl ether, and extracted three times with 25 milliliter portions of CHCl3. The aqueous layer was then removed and dried under vacuum (1.0 mm Hg) for 24 hours. The resulting amorphous solid was then recrystallized from toluene/CHCl3 mixtures to produce the N-(2-carboxyethyl)-2,3,3-trimethylindolinium iodide product as 3.0 grams of a yellow solid (83.5 percent yield). 1H and 13C NMR spectra indicated the following:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06365312B1
출처 데이터셋uspto-grants-2002_04
ORD IDord-3cc345ce49af4f608718e0e9f480376c
출처 메모uspto-grants-2002_04