돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 840233생성일: 2026년 10월 25일

Acetone → 3-(Benzo[1,3]dioxol-5-ylamino)-2-(2,2-dimethyl-propionyl)-3-methylsulfanyl-propenenitrile

https://huagongshe.com/reaction/840233

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물Methyl iodideHCID 6328—
반응물Pentanenitrile, 4,4-dimethyl-3-oxo-HCID 108871—
반응물1,3-Benzodioxole, 5-isothiocyanato-HCID 123593—
생성물3-(Benzo[1,3]dioxol-5-ylamino)-2-(2,2-dimethyl-propionyl)-3-methylsulfanyl-propenenitrileHCID 7015092698%

반응 단계

To a solution of 4,4-dimethyl-3-oxopentanenitrile (0.626 g, 5.0 mmol) in dry acetone (10 ml) first potassium carbonate (1.38 g, 10 mmol) and then 3,4-methylendioxyphenyl isothiocyanate (0.941 g, 5.3 mmol) were added. The resulting mixture was stirred at room temperature under nitrogen for 72 h, and then filtered. To the filtrate methyl iodide (0.93 ml, 15 mmol) was added. The mixture was stirred at room temperature for 45 min. The precipitate was filtered off and the filtrate was concentrated. The residue was taken up into dichloromethane and water. The organic layer was washed with water (2×), dried (sodium sulfate) and concentrated. Crystallisation from ethyl acetate/heptane 1:1 gave 1.56 g (98%) of the title compound. Mp 139-141° C.; 1H NMR (200 MHz, CDCl3): δ=1.40 (s, 9H), 2.28 (s, 3H), 6.03 (s, 2H), 6.75 (dd, 1H), 6.8 (m, 2H), 13.5 (br s, 1H); EI SP/MS: 318 (M+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06365609B1
출처 데이터셋uspto-grants-2002_04
ORD IDord-2d293ca67fa640d18060d813dce05ab2
출처 메모uspto-grants-2002_04