Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Hydrochloric Acid → (4-Allyloxy-3-nitrophenyl)methanol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | 4-Allyloxy-3-nitrobenzaldehyde | HCID 22401152 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | (4-Allyloxy-3-nitrophenyl)methanol | HCID 29006117 | — |
반응 단계
The solution of 2.4 g of 4-allyloxy-3-nitrobenzaldehyde in 30 ml of methanol is cooled to 0° C. with stirring and subsequently admixed with 0.48 g of sodium borohydride in portions over 5 minutes. The reaction mixture is stirred further at 0° C. over 30 minutes, then poured onto cooled 2N HCl (100 ml) and extracted with tert-butyl methyl ether (2×100 ml). The organic phases are washed with water (100 ml), 1M sodium hydrogencarbonate solution (100 ml) and brine (100 ml), dried over sodium sulphate, filtered and concentrated by evaporation. The title compound is obtained as a slightly yellowish oil from the residue by means of flash chromatography (SiO2 60F). Rf=0.12 (1:1 EtOAc-heptane); Rt=3.37.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07790715B2 |
| 출처 데이터셋 | uspto-grants-2010_09 |
| ORD ID | ord-6ce231f443804a51b30a32f22725ea3a |
| 출처 메모 | uspto-grants-2010_09 |