돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 892471생성일: 2026년 10월 24일

Ethyl formate → 2-Formylheptanonitrile

https://huagongshe.com/ko/reaction/892471

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl formateHCID 8025—
반응물HeptanenitrileHCID 12372—
반응물2-Methylpropan-2-olateHCID 4574913—
반응물Potassium tert-butoxideHCID 23665647—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물2-FormylheptanonitrileHCID 1989552977%

반응 단계

A solution of potassium tert-butoxide (18.9 g) in a mixed solvent system of tetrahydrofuran (150 ml) and toluene (100 ml) was heated to 75° . A solution of heptanonitrile (11.2 g) and ethyl formate (24 ml) in toluene (50 ml) was then added dropwise to the warm tert-butoxide solution. The reaction was stirred for 5 hours at 75° then cooled with an ice bath. Ether was added to the mixture and then water. The layers were separated. The aqueous phase was washed once with ether then acidified to a pH of about 3 with aqueous hydrochloric acid (6N). The aqueous phase was saturated with sodium chloride then extracted twice with ether. The combined ether extracts were washed with brine, dried (MgSO4) and concentrated to leave the title product as a yellow oil (10.7 g, 77%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05118688
출처 데이터셋uspto-grants-1992_06
ORD IDord-a43b3531c77943dface0577e8c2daeb0
출처 메모uspto-grants-1992_06