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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 890241생성일: 2026년 10월 26일

2,3-Dichlorobenzoyl chloride → (7-Isopropyl-2-methyl-1H-indol-3-yl)-(2,3-dichlorophenyl)methanone

https://huagongshe.com/reaction/890241

반응식

참여 물질

역할이름HCID투입량
반응물2,3-Dichlorobenzoyl chlorideHCID 17944—
반응물Ammonium ChlorideHCID 25517—
반응물7-isopropyl-2-methyl-1H-indoleHCID 22250590—
반응물HCID 178418573HCID 178418573—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물(7-Isopropyl-2-methyl-1H-indol-3-yl)-(2,3-dichlorophenyl)methanoneHCID 22250583—

반응 조건

온도-30 °C

반응 단계

120 ml of anhydrous THF are cooled to −5° C. and 36 ml of 3M methylmagnesium bromide in ether are added. The mixture is cooled to −30° C. and then 15 g of 7-isopropyl-2-methyl-1H-indole are added dropwise. The mixture is left stirring for 1 hour between −20° C. and −30° C. and then 30.9 g of 2,3-dichlorobenzoyl chloride, dissolved in 120 ml of THF, are added dropwise. The medium is left to return to AT and is then poured onto 300 ml of a saturated NH4Cl solution. Separation is carried out by settling, the organic layer is evaporated and then the residue is taken up in DCM. The organic phase is washed with a saturated NaCl solution and then it is dried and evaporated. The residue is chromatographed on silica while eluting with an AcOEt/cyclohexane (3/7, v/v) mixture.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06995184B2
출처 데이터셋uspto-grants-2006_02
ORD IDord-a970bc18ea78491d8400a8cf48183c82
출처 메모uspto-grants-2006_02