Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Benzyl 2-nitrophenyl ether → 2-Benzyloxyaniline
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Benzyl 2-nitrophenyl ether | HCID 736266 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 촉매 | Nickel Dichloride | HCID 24385 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 2-Benzyloxyaniline | HCID 240548 | 100% |
반응 단계
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).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06756378B2 |
| 출처 데이터셋 | uspto-grants-2004_06 |
| ORD ID | ord-50a53959db354bfd9338cafbe55baa10 |
| 출처 메모 | uspto-grants-2004_06 |