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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55931생성일: 2026년 10월 25일

1-Naphthoic acid → (2-Methyl-1H-indol-3-yl)(naphthalen-1-yl)methanone

https://huagongshe.com/reaction/55931

반응식

참여 물질

역할이름HCID투입량
반응물1-Naphthoic acidHCID 6847—
반응물3-NaphthoylindoleHCID 10355825—
반응물HCID 178418689HCID 178418689—
용매Diethyl EtherHCID 3283—
용매Thionyl ChlorideHCID 24386—
생성물(2-Methyl-1H-indol-3-yl)(naphthalen-1-yl)methanoneHCID 117786841,133.2%

반응 조건

온도0 °C

반응 단계

2-Methylindole 1 (10 g, 76 3 mmol) was dissolved in diethylether (100 ml) under nitrogen atmosphere and cooled to 0° C. MeMgBr (3M) solution (26.7 ml, 80.15 mmol) was added dropwise and allowed to stir at room temperature for 3 hours. In the meantime, 1-naphthoic acid (13.13 g, 76 3 mmol) was dissolved in thionyl chloride (50 ml) and refluxed for 90 min, then the solvent was removed under vacuo and the residue was dissolved in diethylether (50 ml). The resulting solution was added dropwise to the indole reaction mixture at 0° C. and then allowed to stir at room temperature for 2 hours. A solution of ammonium chloride (200 ml) was added to the reaction mixture and the resulting mixture was stirred at room temperature overnight. The solid that was formed was collected by filtration, washed with water and hexane then dried in a dessicator over phosphorous pentoxide to give 9.7 g (45%) (2-methyl-1H-indol-3-yl)(naphthalen-1-yl) methanone 2 as a cream solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434687B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-ba58fb38ded749dba9c0682a8cc39af9
출처 메모uspto-grants-2016_09