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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2107367생성일: 2026년 10월 24일

4-Nitrobenzaldehyde → 1-(4-Nitrophenyl)2-nitro-heptan-1-ol

https://huagongshe.com/ko/reaction/2107367

반응식

참여 물질

역할이름HCID투입량
반응물4-NitrobenzaldehydeHCID 541—
반응물Ethylenediaminetetraacetic AcidHCID 6049—
반응물1-NitrohexaneHCID 12589—
반응물ButyllithiumHCID 178418339—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물1-(4-Nitrophenyl)2-nitro-heptan-1-olHCID 14817329—

반응 단계

n-BuLi (1.6 M in hexane, 6.24 mL) was added dropwise with stirring to a solution of nitrohexane (1.4 mL, 10 mmol) in THF (12 mL) at -78° C. After 15 minutes a solution of TiCl3 (OPriso) (5 mmol) in THF (2 mL) and CH2Cl2 (3 mL) solution was added. After a further 15 minutes 4-nitrobenzaldehyde (0.75 mL, 5 mmol) in CH2Cl2 (3 mL) was added and the mixture allowed to warm up to room temperature (18 30 min.). Stirring was continued for a further 3.5 hours at room temperature and the mixture was quenched with an aqueous slurry of disodium EDTA (1.86 g, 5 mmol) and extracted with Et2O (3×75 mL), aqueous sodium bicarbonate (75 mL) and water (75 mL), dried and evaporated in vacuo. Flash column chromatography [SiO2, hexane:Et2O, 4:1 v/v] gave 1-(4-nitrophenyl)2 -nitro-heptan-1-ol (1.13 g, 81% Erythro:threo ratio 3.9:1

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04933505
출처 데이터셋uspto-grants-1990_06
ORD IDord-7821a067a32a48798f43deb21c16d3d1
출처 메모uspto-grants-1990_06