Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7852생성일: 2026년 10월 24일
2-Butyl-5-methoxy-4-methyl-2-(3-oxopentyl)-1-indanone → butyl-4,8-dimethyl-7-methoxy-1,2,9,9a-tetrahydro-3H-fluoren-3-one
https://huagongshe.com/ko/reaction/7852
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 2-Butyl-5-methoxy-4-methyl-2-(3-oxopentyl)-1-indanone | HCID 21990930 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 용매 | Hydrochloric Acid | HCID 313 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | butyl-4,8-dimethyl-7-methoxy-1,2,9,9a-tetrahydro-3H-fluoren-3-one | HCID 21990871 | — |
반응 단계
A solution of the crude diketone from step 1 in acetic acid (1 mL) and 6N HCl (1 mL) was stirred and heated in an oil bath at 100° C. for 5 hours. After cooling, the reaction mixture was diluted with EtOAc (20 mL), washed with water (10 mL) and brine (10 mL), dried over MgSO4, filtered, and the solvent evaporated under vacuum. The residue was purified by preparative layer chromatography on two 0.1×20×20 cm silica gel GF plates, using 5% EtOAc in CH2Cl2 as developing solvent, to afford 9a butyl-4,8-dimethyl-7-methoxy-1,2,9,9a-tetrahydro-3H-fluoren-3-one (84 mg) as a gum.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07087599B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-619e723c7b9e4e91bac3e3dc222ad9ee |
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| 출처 메모 | uspto-grants-2006_08 |
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