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HRID 37305作成日:2026年10月26日

Cyclododecanecarboxaldehyde → 1-(3-Phenyl-1-propenyl)cyclododecane

https://huagongshe.com/reaction/37305

反応式

関与物質

役割名称HCID仕込み量
反応物CyclododecanecarboxaldehydeHCID 78737—
反応物Phenethyltriphenylphosphonium bromideHCID 10863251—
反応物ButyllithiumHCID 178418339—
溶媒Diethyl EtherHCID 3283—
生成物1-(3-Phenyl-1-propenyl)cyclododecaneHCID 5447171688.2%

反応条件

温度0 °C

反応手順

To 11.4 g (25.5 mmol) of phenylethyl triphenylphosphonium bromide in 50 mL of dry ether at 0° C. is added 10.2 mL (25.5 mmol) of 2.5M butyllithium. The suspension is stirred at 0° C. for 1 hour followed by the addition of 5.0 g (25.5 mmol) of cyclododecane carboxaldehyde. The mixture is stirred at room temperature for 3 hours after which time no starting material is evident by TLC. The reaction mixture is quenched with 1N HCl. The layers are separated and the aqueous layer is washed twice with ethyl ether. The combined organic layers are dried over a MgSO4 and the ether is evaporated. The residue is flash chromatographed on silica gel using hexanes to give 6.4 g of a colorless oil: NMR (CDCl3) δ 1.0-1.6 (m, 10H), 2.6 (m, 1H), 3.4 (d, 2H, J=8 Hz, ), 5.3 (t, 1H, J=7 Hz), 5.45 (q, 1H, J=7 Hz), 7.2 ppm (m, 5H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05420153
出典データセットuspto-grants-1995_05
ORD IDord-3a39a55380c9432ea51b387bb28c73e5
出典メモuspto-grants-1995_05