돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 427374생성일: 2026년 10월 27일

Ethyl bromoacetate → Ethyl [(isoquinolin-5-yl)oxy]acetate

https://huagongshe.com/reaction/427374

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl bromoacetateHCID 7748—
반응물Isoquinolin-5-olHCID 30386—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
용매AcetonitrileHCID 6342—
생성물Ethyl [(isoquinolin-5-yl)oxy]acetateHCID 12902789—

반응 단계

In 10 ml of acetonitrile, 1.0 g of 5-hydroxyisoquinoline and 1.52 ml of ethyl bromoacetate were added in the presence of 2.07 ml of DBU and the resultant mixture was refluxed for 8 hr. The reaction mixture was evaporated under reduced pressure and the resultant residue was redissolved in 1N-HCl, washed with ethyl acetate. The aqueous layer was made alkaline with sodium hydrogencarbonate and extracted with ethyl acetate. The extract was washed with saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate. The dried solution was evaporated under reduced pressure and subjected to a silica gel column chromatography (chloroform) to give 1.46 g of ethyl 5-isoquinolyloxyacetate. The ester was dissolved in 30 ml of ethanol, mixed with 6.5 ml of 1N-NaOH aqueous solution and stirred for 12 hr. The reaction mixture was evaporated under reduced pressure, neutralized by the addition of 1N-HCl and the precipitated crystals were filtered, washed with water and dried to give 0.68 g of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06313094B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-fd144b92d169426d92f7d851759b0230
출처 메모uspto-grants-2001_11