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Benzyl 2-nitrophenyl ether → 2-Benzyloxyaniline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzyl 2-nitrophenyl ether | HCID 736266 | — |
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 触媒 | Nickel Dichloride | HCID 24385 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 2-Benzyloxyaniline | HCID 240548 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06756378B2 |
| 出典データセット | uspto-grants-2004_06 |
| ORD ID | ord-50a53959db354bfd9338cafbe55baa10 |
| 出典メモ | uspto-grants-2004_06 |