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HRID 273965作成日:2026年10月26日

3-Furancarboxaldehyde, 5-(triethylsilyl)- → 4-(1-Hydroxytridecyl)-2-triethylsilylfuran

https://huagongshe.com/reaction/273965

反応式

関与物質

役割名称HCID仕込み量
反応物3-Furancarboxaldehyde, 5-(triethylsilyl)-HCID 10878438—
反応物HCID 178443215HCID 178443215—
溶媒TetrahydrofuranHCID 8028—
生成物4-(1-Hydroxytridecyl)-2-triethylsilylfuranHCID 15663269—

反応手順

Dodecylmagnesium bromide (a 1M solution in tetrahydrofuran; 14.3 ml; 14.3 mmol) was added dropwise to a solution of 2-triethylsilyl-4-furaldehyde (2.0 g, 9.52 mmol) in THF (20 ml) at 0 degrees C. under argon. After stirring at room temperature for 2 hours, the mixture was quenched with dilute HCl and extracted with ethyl ether. Evaporation of the dried (magnesium sulfate) extracts gave an oil, which was purified by flash chromatography on silica using 30% ethyl ether/hexane to give the titled alcohol. 1HNMR (CDCl3) 0.76 (q, 6H, J=8.0 Hz), 0.88 (t, 3H, J=6.3 Hz), 0.98 (t, 9H, J=8.0 Hz), 1.25 (m, 20H), 1.62 (d, 1H, J=4.3 Hz), 1.75 (m, 2H), 4.63 (dd, 1H, J=6.6 Hz, 1.9 Hz), 6.63 (s, 1H) and 7.57 (s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05387606
出典データセットuspto-grants-1995_02
ORD IDord-66d9dbc2c7164687bd1e6c500e1c2450
出典メモuspto-grants-1995_02