돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22933생성일: 2026년 10월 23일

N,N-Dimethylaniline → 2-Phenylindole

https://huagongshe.com/ko/reaction/22933

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DimethylanilineHCID 949—
반응물Bromomethyl 4-methoxyphenyl ketoneHCID 4965—
반응물P-AnisidineHCID 7732—
용매Ethyl AcetateHCID 8857—
생성물2-PhenylindoleHCID 13698—

반응 단계

To a boiling mixture of in-anisidine (1.56 ml, 20.0 minol) and N,N-dimethylaniline (3.5 ml) was added 2-bromo-4-methoxyacetophenone (1.37 g in EtOAc, 6.00 mmol) slowly by syringe. After addition, the mixture was kept at 170° C. for 1 hour. The reaction mixture was cooled to room temperature and a dark colored solid was formed. EtOAc was added along with HCI (2 N). The aqueous layer was extracted with EtOAc several times. The combined organic layers were washed with brine, and dried over MgSO4. Solvent was removed under the reduced pressure to afford a dark brown colored solid. Purification by recrystallization in EtOH afforded indole 31 as a white crystallinc material.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06849656B1
출처 데이터셋uspto-grants-2005_02
ORD IDord-71e649dc94b4468a9952da8d86e5f34c
출처 메모uspto-grants-2005_02