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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7892생성일: 2026년 10월 24일

Hydrochloric Acid → HCID 21990925, 화합물

https://huagongshe.com/ko/reaction/7892

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물1-Hexen-3-oneHCID 15395—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물2-Butyl-6-fluoro-5-methoxy-4-methyl-1-indanoneHCID 21990863—
반응물2-Butyl-6-fluoro-5-methoxy-4-methyl-2-(3-oxohexyl)-1-indanoneHCID 21990865—
용매Acetic AcidHCID 176—
용매TetrahydrofuranHCID 8028—
생성물HCID 21990925HCID 21990925—

반응 조건

온도50 °C

반응 단계

A solution of 2-butyl-6-fluoro-5-methoxy-4-methyl-1-indanone (118 mg, 0.47 mmol) in anhydrous tetrahydrofuran (0.47 mL) was treated with propyl vinyl ketone (0.065 mL, 0.56 mmol) and 1,8-diazabicyclo[5.4.0]undec-7-ene (0.0143 mL, 0.094 mmol). The mixture was stirred and heated in an oil bath at 50° C. for 6 hours and then at room temperature for 64 hours. The solvent was evaporated under vacuum to give a residue consisting mainly of 2-butyl-6-fluoro-5-methoxy-4-methyl-2-(3-oxohexyl)-1-indanone. This material was dissolved in acetic acid (2 mL), treated with aqueous 6N HCl (1.5 mL), and stirred while heating in an 80° C. oil bath for 6 hours. After cooling, the mixture was partitioned between EtOAc (25 mL) and saturated aqueous K2CO3 (25 mL). The organic phase was washed with brine (10 mL), dried over MgSO4, filtered, and evaporated under vacuum to an oil (138 mg). The crude product was purified by preparative layer chromatography on two 0.1×20×20 cm silica gel GF plates, developing with CH2Cl2. The product bands were eluted with EtOAc and the eluent evaporated under vacuum to afford 9a-butyl-4-ethyl-6-fluoro-7-methoxy-8-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one (93 mg) as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087599B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-3bfd2b8db18a4c68b99e3c5c20362e76
출처 메모uspto-grants-2006_08