Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 615930생성일: 2026년 10월 25일
p-Toluenesulfonic acid → 2-(2,6-Dimethylhepta-1,5-dien-1-yl)-4,5-dimethyl-1,3-dithiolane
https://huagongshe.com/reaction/615930
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 반응물 | 3,7-Dimethylocta-2,6-Dienal | HCID 8843 | — |
| 반응물 | 2,3-Butanedithiol | HCID 548353 | — |
| 용매 | Cyclohexane | HCID 8078 | — |
| 생성물 | 2-(2,6-Dimethylhepta-1,5-dien-1-yl)-4,5-dimethyl-1,3-dithiolane | HCID 54508178 | — |
반응 단계
Into a 100 ml reaction flask equipped with spin bar, reflux condenser, heating mantle and hot plate with magnetic stirring apparatus, is placed 0.5 grams para-toluenesulfonic acid, 5.0 ml cyclohexane and 6.1 grams (0.05 moles) of 2,3-butanedithiol. Over a period of 30 minutes with stirring is added to the reaction mass 7.6 grams (0.05 moles) of citral having the structure: ##STR23## After the citral is added, the reaction mass is heated to reflux and refluxed (with removal of water of reaction) over a period of 9 hours. At the end of the 9 hour period, the reaction mass is cooled and transferred to a separatory funnel. The reaction mass is then washed with one 50 ml portion of saturated sodium chloride solution and then dried over anhydrous sodium sulfate, filtered and distilled on a Microvigreux column yielding the following fractions:
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04501904 |
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| 출처 데이터셋 | uspto-grants-1985_02 |
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| ORD ID | ord-bb530340671e4980a242fd11d183fa18 |
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| 출처 메모 | uspto-grants-1985_02 |
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