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HRID 274425作成日:2026年10月26日

Furfural → 1-(Furan-2-yl)pentan-1-ol

https://huagongshe.com/reaction/274425

反応式

関与物質

役割名称HCID仕込み量
反応物FurfuralHCID 7362—
反応物Ammonium ChlorideHCID 25517—
反応物HCID 178418682HCID 178418682—
溶媒TetrahydrofuranHCID 8028—
生成物1-(Furan-2-yl)pentan-1-olHCID 249285—

反応手順

Freshly distilled furfural (233.5 g, 2.43 mol) was dissolved in 200 mL freshly distilled THF and added dropwise to a solution of butylmagnesium bromide (2.0M in THF, 1460 mL, 2.92 mol) at 0° C. under dry nitrogen. After the addition was complete, the mixture was allowed to warm to room temperature overnight. The reaction was recooled to 0° C. and carefully poured into 2 L of cold sat. NH4Cl. The layers were separated, and the aqueous phase was extracted with ether. The combined organic layers were washed with saturated NaCl, dried over MgSO4, evaporated, and vacuum distilled to give 325.6 g (87%): bp 72°-73° C. (0.6 mmHg); 1H NMR (300 MHz, CDCl3) d 7.38 (1H, dd J=1 Hz), 6.33 (1H, m), 6.22 (1H, dd, J=3 Hz), 4.67 (1H, t, J=6 Hz), 2.9 (3H, m), 1.35 (4H, m), 0.90 (3H, t, J=7 Hz); mass spectrum (FAB): 170 (M+NH4).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05389647
出典データセットuspto-grants-1995_02
ORD IDord-2dfc3ac39935421f9ca99a5ac254fa22
出典メモuspto-grants-1995_02