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HRID 1015456作成日:2026年10月27日

Water → 3,3',4,4'-Tetra(hydroxymethyl)-1,1'-biphenyl

https://huagongshe.com/reaction/1015456

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium HydroxideHCID 14798—
反応物5,5'-Bi-2-benzofuran-1,1',3,3'-tetroneHCID 75494—
反応物Aluminium lithium hydrideHCID 21226445—
溶媒TetrahydrofuranHCID 8028—
生成物3,3',4,4'-Tetra(hydroxymethyl)-1,1'-biphenylHCID 5977945355.4%

反応条件

温度100 °C

反応手順

To a solution of 3,3′,4,4′-biphenyltetracarboxylic dianhydride (6.0 g, 20.4 mmol, 1.0 molar equivalent) in THF (600 mL) heated to 100° C. is added carefully a solution of LiAlH4 (1M in tetrahydrofuran) (81 mL, 81.6 mmol, 2.0 molar equivalents). The reaction mixture is stirred overnight at 100° C. To this resulting solution cooled at 0° C. is added a 2M sodium hydroxide solution (50 mL) followed by cold water (25 mL) and THF (50 mL). The reaction mixture is then filtered and concentrated under vacuum. The crude product is then washed with THF (20 mL), water (10 mL) and dried over vacuum to give a white powder (3.1 g, 55%). If necessary, the compound can be further purified by recrystallisation in water to give the expected compound as a white powder (3.3 g, 79%). 1H NMR (300.13 MHz, DMSO) δ (ppm) 4.57 (d, J=4.5 Hz, 4H) 4.61 (d, J=4.5 Hz, 4H) 5.09 (t, J=5.2 Hz, 2H) 5.15 (t, J=5.2 Hz, 2H) 7.46 (d, J=8.1 Hz, 2H) 7.52 (dd, J1=8.1, J2=1.8 Hz, 2H) 7.70 (d, J=1.8 Hz, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07985353B2
出典データセットuspto-grants-2011_07
ORD IDord-0b120b38b3e34726a7fba2593289fbf9
出典メモuspto-grants-2011_07