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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1111880생성일: 2026년 10월 27일

Acetic Acid → N-(1-ethylpropyl)-3,4-dimethylaniline

https://huagongshe.com/reaction/1111880

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물3,4-DimethylanilineHCID 7248—
반응물Ethyl ketoneHCID 7288—
반응물Sodium cyanoborohydrideHCID 5003444—
용매MethanolHCID 887—
생성물N-(1-ethylpropyl)-3,4-dimethylanilineHCID 9198497.5%

반응 단계

A solution of 3,4-xylidine (1.2 g., 0.01 mole) and diethyl ketone (5 ml.) in methanol (20 ml.) is stirred at room temperature in the presence of sodium cyanoborohydride (1.1 g.) and 3A molecular sieves (3.0 g.). The pH is monitored each half hour and maintained at 6 by adding acetic acid in 5 drop portions as required. After 7 hours, the sieves are removed by filtration and the filtrate is diluted with water (100 ml.) and then acidified with hydrochloric acid. The solution is then basified with solid potassium carbonate and extracted with ethyl ether. The ether solution is dried and then evaporated leaving the desired product as a residual oil in 97.5% yield and in 93% purity as determined by gas-liquid chromatography. The compound had a boiling point of 80° C. at a pressure of 0.1 mm. Its elemental analysis is as follows:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04119669
출처 데이터셋uspto-grants-1978_10
ORD IDord-429832637d804aeaa090bbcde588d6eb
출처 메모uspto-grants-1978_10