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HRID 354337作成日:2026年10月26日

Benzyl 2-nitrophenyl ether → 2-Benzyloxyaniline

https://huagongshe.com/reaction/354337

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl 2-nitrophenyl etherHCID 736266—
反応物Sodium borohydrideHCID 4311764—
触媒Nickel DichlorideHCID 24385—
溶媒MethanolHCID 887—
生成物2-BenzyloxyanilineHCID 240548100%

反応手順

To a stirred solution of 2-benzyloxynitrobenzene (9.92 g, 43.3 mmol) and NiCl2 (20.3 g, 157 mmol) in MeOH (350 mL) was added portionwise NaBH4 (8.09 g, 214 mmol) at 0° C. After disappearing of the starting material (monitored by TLC), the mixture was evaporated off. The black precipitate was dissolved in 1N HCl, then acidic solution was alkalified by the addition of 1N NaOH and extracted with EtOAc. The extracts were washed brine, dried over Na2SO4, and concentrated to dryness. Chromatography of the residue with CHCl3 as eluent gave 2-benzyloxy aniline (8.60 g, 100%) as a reddish oil. 1H-NMR (CDCl3) δ3.71 (broad s, 2H), 5.06 (s, 2H), 6.68-6.86 (m, 4H), 7.32-7.44 (m, 5H); FAB-MS m/z 200 (M++1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06756378B2
出典データセットuspto-grants-2004_06
ORD IDord-50a53959db354bfd9338cafbe55baa10
出典メモuspto-grants-2004_06