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HRID 2276377作成日:2026年10月25日

Allyl bromide → HCID 66705960、化合物

https://huagongshe.com/reaction/2276377

反応式

関与物質

役割名称HCID仕込み量
反応物Allyl bromideHCID 7841—
反応物Sodium hydrideHCID 24758—
反応物(-)-1-(4-Fluorophenyl)ethanolHCID 852997—
溶媒DimethylformamideHCID 6228—
生成物HCID 66705960HCID 6670596080%

反応手順

To a stirred suspension of sodium hydride (3.14 g, 55% dispersion in oil) in dry DMF (180 ml) under an argon atmosphere was added (S)-1-(4-fluorophenyl)-ethanol (8.41 g, CAS 101219-73-2). Allyl bromide (6.6 ml) was then added dropwise. The reaction mixture was stirred for 30 min at room temperature and was then quenched by addition of water. The mixture was extracted with ethyl acetate twice. The combined organic layers were dried (MgSO4) and concentrated in vacuo. The crude product was purified by column chromatography (SiO2; gradient: heptane/EtOAc) to give 1-((S)-1-allyloxy-ethyl)-4-fluoro-benzene (8.66 g, 80%) as a colourless liquid. 1H NMR (300 MHz, CDCl3, δ ppm): 1.43 (d, J=6.6 Hz, 3H), 3.84 (m, 2H), 4.45 (q, J=6.6 Hz, 1H), 5.15 (dd, J1=10.5 Hz, J2=1.8 Hz, 1H), 5.22 (dd, J1=17.4 Hz, J2=1.8 Hz, 1H), 5.89 (m, 1H), 7.03 (m, 2H), 7.29 (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09132136B2
出典データセットuspto-grants-2015_09
ORD IDord-74ccacda75ef4b36acfee4bf7b142e12
出典メモuspto-grants-2015_09