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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18630생성일: 2026년 10월 25일

Dicyclohexylcarbodiimide → 4-(5-thioxo-5H-1,2-dithiol-3-yl)phenyl 2-(2-methoxynaphthalen-6-yl)propanoate

https://huagongshe.com/reaction/18630

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물NaproxenHCID 156391—
반응물Desmethylanethol trithioneHCID 3082127—
반응물HCID 178418300HCID 178418300—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물4-(5-thioxo-5H-1,2-dithiol-3-yl)phenyl 2-(2-methoxynaphthalen-6-yl)propanoateHCID 2506598636%

반응 조건

온도0 °C

반응 단계

To the solution of 1 (naproxen, 595 mg, 2.58 mmol) in 20 mL of dimethylformamide, hydroxybenzotriazole (388 mg, 2.87 mmol) and DCC (593 mg, 2.87 mmol) were added with stirring at 0° C. for 1 h. To the reaction mixture 5-p-hydroxyphenyl-1,2-dithiole-3-thione (2; 650 mg, 2.87 mmol) was added and stirred for 1 h at 0° C. and 2 h at room temperature. After filtration, the filtrate was evaporated under reduced pressure to remove the solvent. The oily residue thus obtained was dissolved in ethyl acetate; the organic layer was washed with brine, with NaHCO3 5%, with citric acid 10% and than dried on anhydrous MgSO4, filtered and the solvent evaporated. The crude product was loaded on a silica gel open column and eluted with dichloromethane, from which 4-(5-thioxo-5H-1,2-dithiol-3-yl)phenyl 2-(2-methoxynaphthalen-6-yl)propanoate (3) was obtained (406 mg, 36% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741359B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-ed9d067180cb45dbad0b2c6c6c38e597
출처 메모uspto-grants-2010_06