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HRID 1792130作成日:2026年10月27日

3-(3-Quinolyl)-2-propyn-1-ol t-butyl carbonate → 3-(3-Quinolyl)-2-propen-1-ol t-butyl carbonate

https://huagongshe.com/reaction/1792130

反応式

関与物質

役割名称HCID仕込み量
反応物3-(3-Quinolyl)-2-propyn-1-ol t-butyl carbonateHCID 131723396—
触媒PalladiumHCID 23938—
触媒Lindlars catalystHCID 131709914—
溶媒IsopropanolHCID 3776—
生成物3-(3-Quinolyl)-2-propen-1-ol t-butyl carbonateHCID 86584259—

反応手順

To a 250-mL single-necked round-bottom flask was charged the 3-(3-quinolyl)-2-propyn-1-ol t-butyl carbonate (1.52 g, 5.37 mmol), isopropanol (30 mL) and 5% palladium on calcium carbonate poisoned with lead (Lindlar's catalyst, 75 mg, 0.049 equiv). The suspension was stirred (rapidly) magnetically and the atmosphere above the solution was purged with hydrogen. A balloon of hydrogen gas was then placed over the reaction stirring mixture and the reaction was allowed to stir for 16 hours at room temperature. The reaction mixture was then filtered through a 0.45μ filter disk and rinsed with 10 mL of isopropanol. The combined filtrates were concentrated under reduced pressure and the residue (1.55 g) was taken up in 9 mL of heptane/acetone (8:1) and eluted through a plug of silica gel (1.5 g) with 8:1:0.01 heptane/acetone/triethylamine. The desired fractions were combined and concentrated under reduced pressure to provide 3-(3-quinolyl)-2-propen-1-ol t-butyl carbonate: 1.1 g, 71.9%

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07074932B2
出典データセットuspto-grants-2006_07
ORD IDord-b409aa7fda1e49bbb7bfb0b9464b3638
出典メモuspto-grants-2006_07