Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 51161생성일: 2026년 10월 23일
1,1,7-Trimethyl-1,2,3,4-tetrahydronaphthalene → 4,4,6-Trimethyl-1,2,3,4-tetrahydronaphthalen-1-one
https://huagongshe.com/ko/reaction/51161
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 1,1,7-Trimethyl-1,2,3,4-tetrahydronaphthalene | HCID 226396 | — |
| 반응물 | Potassium Bromate | HCID 23673461 | — |
| 반응물 | Ammonium cerium-nitrate | HCID 57418452 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 4,4,6-Trimethyl-1,2,3,4-tetrahydronaphthalen-1-one | HCID 13463267 | 89% |
반응 단계
A solution of 1,2,3,4-tetrahydro-1,1,7-trimethyl-naphthalene (9.60 g, 55 mmol), potassium bromate (9.17 g, 55 mmol), cerium ammonium nitrate (1.50 g) in water (28 mL) and dioxane (44 mL) was heated under argon at 85° C. for 6 hours. The mixture was then cooled to 0° C., diluted with ethyl acetate and water. The organic phase was separated and the aqueous phase extracted with ethyl acetate. The combined organic extracts were washed with water (2×), saturated sodium bicarbonate and brine, dried over anhydrous magnesium sulfate, filtered and concentrated. The residue was purified by silica gel chromatography (6.5×17 cm, 10% ethyl acetate/hexane) to give the title material (9.2 g, 89%) as a colorless oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06713515B2 |
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| 출처 데이터셋 | uspto-grants-2004_03 |
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| ORD ID | ord-5a6a05f22504482d946a9a88e8cb4b00 |
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| 출처 메모 | uspto-grants-2004_03 |
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