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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1816544생성일: 2026년 10월 26일

Hydrochloric Acid → O-benzyl-N-(2,4,6-trimethoxy-benzyl)hydroxylamine

https://huagongshe.com/reaction/1816544

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium HydroxideHCID 14798—
반응물2,4,6-TrimethoxybenzaldehydeHCID 70019—
반응물O-BenzylhydroxylamineHCID 102313—
반응물Sodium cyanoborohydrideHCID 5003444—
용매DichloromethaneHCID 6344—
생성물O-benzyl-N-(2,4,6-trimethoxy-benzyl)hydroxylamineHCID 2249497983%

반응 단계

2,4,6-Trimethoxybenzaldehyde (12.42 g, 63.3 mmol) and O-benzylhydroxylamine (7.80 g, 63.3 mmol) were stirred in dichloromethane (65 mL) at rt overnight. The solvent was removed under reduced pressure. The crude residue was dissolved in ethanol (550 mL) and sodium cyanoborohydride (12.0 g, 189.9 mmol) was added dropwise. The mixture was stirred for 5-10 min, then 12 N HCl was added dropwise until pH became below 3. The reaction mixture was stirred for additional 3 h and 1 N NaOH was added until pH>8. The product was extracted with dichloromethane. The organic phase was dried over Na2SO4 and concentrated under vacuo. The residue was purified by flash chromatography (5% ether in dichloromethane) to give 15.9 g of O-benzyl-N-(2,4,6-trimethoxy-benzyl)hydroxylamine as an oil (83% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06884907B2
출처 데이터셋uspto-grants-2005_04
ORD IDord-c82029e8226e4b60aef08c7dc6342d43
출처 메모uspto-grants-2005_04