돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1289020생성일: 2026년 10월 27일

Butyl methyl ether → 3-(2-Benzyloxyethoxy)-4-methoxybenzyl ethyl ketone

https://huagongshe.com/reaction/1289020

반응식

참여 물질

역할이름HCID투입량
반응물Butyl methyl etherHCID 12338—
반응물Butanoic acid, 2-bromo-, ethyl esterHCID 79039—
반응물Sodium MethoxideHCID 10942334—
반응물3-(2-Benzyloxyethoxy)-4-methoxy-benzaldehydeHCID 21716329—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
생성물3-(2-Benzyloxyethoxy)-4-methoxybenzyl ethyl ketoneHCID 18925346—

반응 단계

24 g of the product of step (ii) 21.5 g bromobutyric acid ethyl ester and 30 ml t.butyl methyl ether are added dropwise over 50 mins. at 5° C. to a pre-prepared suspension of sodium methylate in 25 ml t.butyl methyl ether. The reaction mixture is stirred for 45 mins. at ca. 5° C. and then stirred for 12 hrs. at room temperature. The pH is adjusted to 5 by addition of glacial acetic acid and the obtained suspension diluted with H2O and extracted 3× with t.butyl methyl ether. The organic phase is extracted with NaHCO3 (1×) and brine (1×), and evaporated to ca. 100 ml. 13.5 ml 50% aqueous NaOH are added drop-wise and the whole stirred for 2 hrs. at 40° C., diluted with 50 ml. H2O and stirred for a further 30 mins. at room temperature. The organic phase is separated and the aqueous phase adjusted to pH 1 at max. 40° C. with 15 ml conc. HCl. The reaction mixture is stirred at 40° C. for a further 1.5 hrs., cooled to room temperature and extracted with toluene. The organic phase is washed with NaHCO3 and brine, dried over Na2SO4, filtered and evaporated to yield the title compound as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05747506
출처 데이터셋uspto-grants-1998_05
ORD IDord-65e29963b8bb4ab7b552258883b5b431
출처 메모uspto-grants-1998_05