돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1075329생성일: 2026년 10월 25일

3-(Methoxymethyl)-4-methylaniline → N-(1-ethylpropyl)-3-(methoxymethyl)-p-toluidine

https://huagongshe.com/reaction/1075329

반응식

참여 물질

역할이름HCID투입량
반응물3-(Methoxymethyl)-4-methylanilineHCID 12767667—
용매Ethyl ketoneHCID 7288—
생성물N-(1-ethylpropyl)-3-(methoxymethyl)-p-toluidineHCID 12767668119%

반응 단계

A mixture of 3-(methoxymethyl)-p-toluidine (9.3 g), 5 angstrom molecular sieves (19 g) and diethyl ketone (40 ml) is stirred at room temperature for 15 hours. The mixture is then filtered. Additional diethyl ketone (10-15 ml) and molecular sieves (10 g) are added to the filtrate. After 40 minutes at 40° to 50° C., the reaction mixture is filtered and then concentrated under vacuum. The crude product (9.0 g) is dissolved in methanol (50 ml) and cooled to 10° C. Sodium borohydrate (3.7 g) and methanol (25 ml) are simultaneously added in small portions. Thirty minutes after these additions, the mixture is acidified with 10% hydrochloric acid while in an ice bath. The mixture is extracted with ether and the ether extract is discarded. The aqueous extract is made alkaline and then extracted with ether. The ether extract is dried over magnesium sulfate and concentrated to yield 8.1 g of an orange oil which is more than 97% homogeneous as estimated by gas-liquid chromatography. Fractional distillation yields a product having a boiling point of 120° to 125° C. at 0.4 to 0.5 mm pressure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04395577
출처 데이터셋uspto-grants-1983_07
ORD IDord-01fea57a10ef4baebaedc48701c58ef0
출처 메모uspto-grants-1983_07