돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 127498생성일: 2026년 10월 25일

Acetic Anhydride → Alphanitro-6-chloro-3-indoleacrylic acid methylester

https://huagongshe.com/reaction/127498

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물6-ChloroindoleHCID 87111—
반응물alpha-Nitro-beta-ethoxyacrylic acid methylesterHCID 53395203—
생성물Alphanitro-6-chloro-3-indoleacrylic acid methylesterHCID 5374664451%

반응 단계

A 4-1. battery jar was charged with 641 g (4.23 moles) of 6-chloroindole, 926 g (5.3 moles) of crude (ca. 85% pure) alpha-nitro-beta-ethoxy acrylic acid methylester and 475 L g (4.65 moles) of acetic anhydride. The mixture was well stirred at room temperature for 45 hours to give a highly viscous suspension of an orange precipitate. 1.5 l of a mixture of benzene-ether-hexane 1:1:3 was added and the mixture stirred vigorously for 30 minutes. The product was collected by filtration, washed with 1.0 l of the same solvent mixture and dried at room temperature and 16 mmHg to constant weight to afford 600 g (51%) of product as orange crystals, m.p. 159°-160°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04256641
출처 데이터셋uspto-grants-1981_03
ORD IDord-cd9b77a451e04e88b7d5f464f6d58049
출처 메모uspto-grants-1981_03