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HRID 129532作成日:2026年10月26日

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

https://huagongshe.com/reaction/129532

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, 5

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05468774
出典データセットuspto-grants-1995_11
ORD IDord-c1a0464607584b3bbe40ecd0acae5021
出典メモuspto-grants-1995_11