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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 462571생성일: 2026년 10월 24일

Phenylacetaldehyde → 2-Benzyl-4,5-Dimethyl-1,3-Dithiolane

https://huagongshe.com/ko/reaction/462571

반응식

참여 물질

역할이름HCID투입량
반응물PhenylacetaldehydeHCID 998—
반응물p-Toluenesulfonic acidHCID 6101—
반응물CyclohexaneHCID 8078—
반응물2,3-ButanedithiolHCID 548353—
용매WaterHCID 962—
생성물2-Benzyl-4,5-Dimethyl-1,3-DithiolaneHCID 20398675—

반응 단계

Into a 100 ml flask equipped with reflux condenser and magnetic stirring bar and hot plate equipped with magnetic stirring apparatus is placed 0.2 grams of para-toluenesulfonic acid, 5 ml cyclohexane and 6.1 grams (0.05 moles) of 2,3-butanedithiol. With stirring, over a period of 30 minutes, 6.0 grams (0.05 moles) of phenylacetaldehyde is added to the reaction mass. The reaction mass is then heated to reflux and refluxed for a period of 10 hours during which time water of formation is removed. After the 10 hour period, the reaction mass is cooled and transferred to a separatory funnel. The reaction mass is washed with one 50 ml portion of saturated sodium chloride, dried over anhydrous sodium sulfate and filtered. The resulting filtrate is then distilled on a Microvigreux column yielding the following four fractions:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04515968
출처 데이터셋uspto-grants-1985_05
ORD IDord-be3009770ae34e7aa9fa1040ba40f2e6
출처 메모uspto-grants-1985_05