Hydrochloric Acid → HCID 21990925, 화합물

온도

50 °C

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.

1. customThe solvent was evaporated under vacuum
2. customto give a residue
3. stirringstirred
4. temperaturewhile heating in an 80° C. oil bath for 6 hours
5. temperatureAfter cooling
6. customthe mixture was partitioned between EtOAc (25 mL) and saturated aqueous K2CO3 (25 mL)
7. washThe organic phase was washed with brine (10 mL)
8. dry with materialdried over MgSO4
9. filtrationfiltered
10. customevaporated under vacuum to an oil (138 mg)
11. customThe crude product was purified by preparative layer chromatography on two 0.1×20×20 cm silica gel GF plates
12. washThe product bands were eluted with EtOAc
13. customthe eluent evaporated under vacuum

ORD 기록

ord-3bfd2b8db18a4c68b99e3c5c20362e76

출처 데이터셋

uspto-grants-2006_08

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US07087599B2