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HRID 1419952作成日:2026年10月25日

Allyl iodide → (trans)-N-[[2-[3-(2-Propenyloxy)phenyl]cyclopropyl]methyl]butanamide

https://huagongshe.com/reaction/1419952

反応式

関与物質

役割名称HCID仕込み量
反応物Allyl iodideHCID 11166—
反応物Potassium HydroxideHCID 14797—
反応物HCID 70274674HCID 70274674—
反応物(trans)-N-[[(2-Propen-1-yloxyphenyl)cyclopropyl]methyl]butanamideHCID 86754003—
溶媒EthanolHCID 702—
溶媒Diethyl EtherHCID 3283—
生成物(trans)-N-[[2-[3-(2-Propenyloxy)phenyl]cyclopropyl]methyl]butanamideHCID 1586031334%

反応手順

(trans)-N-[[(2-Propen-1-yloxyphenyl)cyclopropyl]methyl]butanamide: To a rapidly stirred solution of (trans)-N-[[2-(3 hydroxyphenyl)cyclopropyl]methyl]butanamide (0.8 g, 3.4 mmol) and KOH (210 mg, 3.74 mmol) in ethanol (15 mL) was added allyl iodide (622 mg, 3.7 mmol). After stirring for 18 h, the suspension was diluted with Et2O (100 mL), and washed with H2O, 2N NaOH, brine, dried (K2CO3), and concentrated to a give a crude residue. The resulting material was purified by chromatography (silica gel, 40% EtOAc/hexane) to afford 320 mg (34%) of the title compound: 1H NMR (300 MHz, CDCl3) δ 0.70-0.94 (m, 5H), 1.12-1.32 (m, 1H), 1.58-1.84 (m, 3H), 2.20 (t, J=6.0 Hz, 2H), 3.15-3.36 (m, 2H), 4.48 (d, J=5.6 Hz, 2H), 5.24 (d, J=10.0 Hz, 1H), 5.40 (d, J=17.2 Hz, 1H), 5.56 (br s, 1H), 5.96-6.07 (m, 1H), 6.57-6.70 (m, 3H), 7.13 (t, J=7.2 Hz, 1H); IR (NaCl Film) 3296, 2962, 1644, 1607, 1548, 1494 cm-1 ; MS m/e 273; Analysis calc'd for C17H23NO2 0.20(H2O): C, 73.72; H, 8.52; N, 5.06; found: C, 73.77; H, 8.63; N, 5.00.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05889031
出典データセットuspto-grants-1999_03
ORD IDord-e594b70a9799491e805fd8fde2031cec
出典メモuspto-grants-1999_03