돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1808672생성일: 2026년 10월 26일

Methyl cyanoacetate → Indole

https://huagongshe.com/reaction/1808672

반응식

참여 물질

역할이름HCID투입량
반응물Methyl cyanoacetateHCID 7747—
반응물PiperidineHCID 8082—
반응물1H-Indole-3-carboxaldehyde, 1-methyl-2-phenyl-HCID 74468—
용매MethanolHCID 887—
생성물IndoleHCID 798263.8%

반응 단계

To 120 ml of methanol were added 23.5 g (0.10 mol) of 1-methyl-2-phenyl-1H-indole-3-carbaldehyde and 11.9 g (0.12 mol) of methyl cyanoacetate to produce a mixture. Subsequently, 2.5 g (0.03 mol) of piperidine was added to the mixture, reacted under reflux for 6 hours, and cooled to room temperature to precipitate a crystal. The obtained crystal was washed with a small amount of methanol, and then dried to give 30.9 g of a light-yellow crystalline indole compound A having a structure of the general Chemical Formula (1) in which R1 was methyl group and R2 was methyl group. The melting point of the obtained indole compound A was 193.7° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08361625B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-49669eb5cbd143bb9afba59f582bd187
출처 메모uspto-grants-2013_01