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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1712251생성일: 2026년 10월 27일

Hydrochloric Acid → (4-Allyloxy-3-nitrophenyl)methanol

https://huagongshe.com/reaction/1712251

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium borohydrideHCID 4311764—
반응물4-Allyloxy-3-nitrobenzaldehydeHCID 22401152—
용매MethanolHCID 887—
생성물(4-Allyloxy-3-nitrophenyl)methanolHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07790715B2
출처 데이터셋uspto-grants-2010_09
ORD IDord-6ce231f443804a51b30a32f22725ea3a
출처 메모uspto-grants-2010_09