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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 328354생성일: 2026년 10월 27일

Hydroxyurethane → N-carboethoxy-O-(2,4,6-trimethylbenzyl)hydroxylamine

https://huagongshe.com/reaction/328354

반응식

참여 물질

역할이름HCID투입량
반응물HydroxyurethaneHCID 11510—
반응물Potassium HydroxideHCID 14797—
반응물2,4,6-Trimethylbenzyl chlorideHCID 74108—
반응물PotassiumHCID 5462222—
생성물N-carboethoxy-O-(2,4,6-trimethylbenzyl)hydroxylamineHCID 2144181053.8%

반응 단계

50 ml of a methanolic solution of 12.3 g (0.22 mole) of potassium hydroxide was added to 50 ml of an ice-cooled methanolic solution of 23.1 g (0.22 mole) of N-carboethoxyhydroxylamine to prepare a solution containing a potassium salt of N-carboethoxyhydroxylamine, and 50 ml of a methanolic solution of 33.7 g (0.2 mole) of 2,4,6-trimethylbenzyl chloride was added to the resulting solution at room temperature. The resulting mixture was heated under refluxing for 1 hour, and the solvent was distilled off. 150 ml of diethyl ether and 50 ml of water were then added to the residue and the organic layer was separated, dried over anhydrous sodium sulfate and concentrated under a reduced pressure. The residue thus obtained was distilled under a reduced pressure to obtain 25.5 g (53.8% yield) of substantially pure N-carboethoxy-O-(2,4,6-trimethylbenzyl)hydroxylamine having a boiling point of 148°-153° C/0.9 mmHg.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04017512
출처 데이터셋uspto-grants-1977_04
ORD IDord-aefd2ebf1ba44294a55a17ee2a194edc
출처 메모uspto-grants-1977_04