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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2357141생성일: 2026년 10월 25일

Formaldehyde → 2-(4-Methoxycarbonyl-2-nitrophenyl)propanol

https://huagongshe.com/reaction/2357141

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물Methyl 4-ethyl-3-nitrobenzoateHCID 21938352—
반응물Potassium tert-butoxideHCID 23665647—
용매Dimethyl SulfoxideHCID 679—
생성물2-(4-Methoxycarbonyl-2-nitrophenyl)propanolHCID 6845417938%

반응 단계

To a suspension of 4-ethyl-3-nitrobenzoic acid methyl ester (11d) (10 g, 48 mmol) and paraformaldehyde (1.8 g, 60 mmol) in DMSO (10 mL) was added in portions potassium tert-butoxide (1.46 g, 12 mmol), during which the colour of the reaction mixture was changing from yellow to purple. After stirring for 2.5 hours at room temperature, the reaction mixture was directly applied to the silica gel bed of a chromatography column (100 g silica, 3.5×14 cm) and eluted with hexane/ethyl acetate (EA) (3:1, v/v). The slightly yellow product (4d) was obtained in 38% yield (4.42 g, 18 mmol). Rf=0.24 (hexanes/EtOAc 7:3). 1H NMR (250 MHz, CDCl3) δ 8.36 (d, 1H, arom. H(3)), 8.18 (dd, 1H, arom. H(5)), 7.58 (d, 1H, arom. H(6)), 3.93 (s, 3H, COOCH3), 3.78 (m, 2H, α-CH2), 3.54 (sextet, 1H, β-CH), 1.69 (d, 3H, CH3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07759513B2
출처 데이터셋uspto-grants-2010_07
ORD IDord-d0615736ac9f47c38178b868218079ba
출처 메모uspto-grants-2010_07