戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1992870作成日:2026年10月25日

1-Hexyne → HCID 68534753、化合物

https://huagongshe.com/reaction/1992870

反応式

関与物質

役割名称HCID仕込み量
反応物1-HexyneHCID 12732—
反応物Ammonium ChlorideHCID 25517—
反応物DiisopropylethylamineHCID 81531—
反応物Methyl 4-methoxy-2-(trifluoromethylsulfonyloxy)benzoateHCID 10710352—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒HCID 178418476HCID 178418476—
溶媒DimethylformamideHCID 6228—
生成物HCID 68534753HCID 6853475398%

反応手順

To a degassed solution of methyl 4-(methyloxy)-2-{[(trifluoromethyl)sulfonyl]oxy}benzoate (77) (0.72 g, 2.30 mmol), Pd(PPh3)2Cl2 (0.16 g, 0.23 mmol), CuI (44 mg, 0.23 mmol), diisopropylethylamine (1.41 mL, 8.02 mmol) in DMF (10 mL) at room temperature was added 1-hexyne (0.55 mL, 4.60 mmol). The mixture was stirred at room temperature overnight. Poured into saturated aqueous NH4Cl (15 mL), the mixture was extracted with EtOAc. The combined organic extract was washed with water, brine, dried over Na2SO4, filtered, and the filtrate was concentrated to give the crude product as a dark brown oil. The crude product was purified by flash chromatography over SiO2 eluted with a gradient from hexanes to 5% EtOAc in hexanes to give 0.55 g (98%) of 78 as a light brown oil. 1H NMR (400 MHz, CDCl3): δ 0.95 (t, J=7.2 Hz, 3H), 1.45-1.58 (m, 2H), 1.60-1.70 (m, 2H), 2.48 (t, J=7.2 Hz, 2H), 3.83 (s, 3H), 3.87 (s, 3H), 6.82 (dd, J1=8.9 Hz, J2=2.6 Hz, 1H), 6.98 (d, J=2.5 Hz, 1H), 7.88 (d, J=8.8 Hz, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07649093B2
出典データセットuspto-grants-2010_01
ORD IDord-2957a998d06c4fa3a7f990b2702d8f5c
出典メモuspto-grants-2010_01