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HRID 16225作成日:2026年10月26日

4-Pentenal → 1,8-Nonadien-5-ol

https://huagongshe.com/reaction/16225

反応式

関与物質

役割名称HCID仕込み量
反応物4-PentenalHCID 16418—
反応物HCID 178418797HCID 178418797—
溶媒TetrahydrofuranHCID 8028—
生成物1,8-Nonadien-5-olHCID 11829542—

反応手順

3-Butenyl-magnesium bromide (125 mL, 0.5 M in tetrahydrofuran, 62.5 mmol) was added drop wise to a stirred and cooled (−78° C.) solution of pent-4-enal (4 g, 48.07 mmol) in dry tetrahydrofuran (160 mL). After the addition, the solution was warmed to room temperature and then quenched with NH4Cl solution. The mixture was partitioned with diethyl ether and the organic phase was washed with brine, dried (MgSO4), filtered, and evaporated. The residue was purified over silica gel using 5-15% diethyl ether in hexanes to give the title compound as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737137B2
出典データセットuspto-grants-2010_06
ORD IDord-e98f6149fafa44c789cdbd4327d485dc
出典メモuspto-grants-2010_06