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HRID 711812作成日:2026年10月25日

Sodium borohydride → 2-(Hydroxymethyl)-6-nitrobenzonitrile

https://huagongshe.com/reaction/711812

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium borohydrideHCID 4311764—
反応物2-Formyl-6-nitrobenzonitrileHCID 86657474—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物2-(Hydroxymethyl)-6-nitrobenzonitrileHCID 67401034—

反応手順

Sodium borohydride (92.0 mg, 2.43 mmol) was added to a solution of 2-formyl-6-nitrobenzonitrile (Example 207e) (0.86 g, 4.88 mmol) in MeOH (38 mL) and THF (38 mL) at −8° C., and was stirred at that temperature for no more than 30 min. The reaction was quenched with HCl (6 M, 4.88 mL), followed by addition of water (50 mL), and brine (50 mL). The mixture was extracted with EtOAc, the combined extract was dried over MgSO4, filtered and concentrated. The crude product was purified by chromatography on silica using the solvent gradient CH2Cl2→CH2Cl2/MeOH (8:2) to give the title compound in amount of 0.32 g, (37%), which was used immediately in the next step. 1H NMR (400 MHz, DMSO-d6) δ 4.77 (d, J=5.6 Hz, 2H), 5.87 (t, J=5.6 Hz, 1H), 7.97 (t, J=8.0 Hz, 1H), 8.07 (dd, J=0.4, 8.0 Hz, 1H), 8.28 (dd, J=0.8, 8.0 Hz, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09181276B2
出典データセットuspto-grants-2015_11
ORD IDord-e24b00fc7cbf43b7a2da0fd7ec13bd6e
出典メモuspto-grants-2015_11