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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 376961생성일: 2026년 10월 26일

1,3-Propanedithiol → 1-[4-(3-Mercaptopropylthio)phenyl]-2-dimethylamino-2-benzyl-butan-1-one

https://huagongshe.com/reaction/376961

반응식

참여 물질

역할이름HCID투입량
반응물1,3-PropanedithiolHCID 8013—
반응물Potassium CarbonateHCID 11430—
반응물2-Benzyl-2-(dimethylamino)-1-(4-fluorophenyl)butan-1-oneHCID 19360599—
용매DimethylacetamideHCID 31374—
생성물1-[4-(3-Mercaptopropylthio)phenyl]-2-dimethylamino-2-benzyl-butan-1-oneHCID 19360633—

반응 조건

온도50 °C

반응 단계

32.5 g (0.3 mol) of 1,3-propanedithiol are dissolved in 50 ml of dry dimethylacetamide, and the solution is heated to about 50° C. together with 13.8 g (0.1 mol) of potassium carbonate. 15.0 g (0.05 mol) of 1-(4-fluorophenyl)-2-dimethylamino-2-benzyl-butan-1-one in 30 ml of dry dimethylacetamide are added dropwise. The suspension is stirred at 50° C. overnight (about 12 hours), then the solid is filtered off. The excess 1,3-propanedithiol and dimethylacetamide are distilled off. To the residue is added toluene, then the precipitate is filtered off. After distilling off the toluene, the residue is purified by means of column chromatography on silica gel with ethyl acetate-hexane (1:7) as an eluent, and an oily product is obtained. The structure is confirmed by the 1H-NMR spectrum (CDCl3): δ [ppm]: 0.68 (t, 3H), 1.39 (t, 1H), 1.79-1.88 (m, 1H), 1.97-2.11 (m, 3H), 2.36 (s, 6H), 2.69 (q, 2H), 3.12 (t, 2H), 3.19 (s, 2H), 7.15-7.27 (m, 7H), 8.28 (d, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06022906
출처 데이터셋uspto-grants-2000_02
ORD IDord-cab446e251fe4108813cf01645b94b33
출처 메모uspto-grants-2000_02