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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1374965생성일: 2026년 10월 26일

Hydrochloric Acid → 1-(4-Isopropoxyphenyl)-1H-indole-2,3-dione

https://huagongshe.com/reaction/1374965

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물IsatinHCID 7054—
반응물TriethylamineHCID 8471—
반응물Sodium BicarbonateHCID 516892—
반응물4-Isopropoxybenzeneboronic acidHCID 3698726—
촉매Cupric acetateHCID 8895—
용매DichloromethaneHCID 6344—
생성물1-(4-Isopropoxyphenyl)-1H-indole-2,3-dioneHCID 2107938339.7%

반응 단계

A solution of triethylamine (28 g, 272 mmol) in CH2Cl2 (250 mL) was added to a mixture of 1H-indole-2,3-dione (10.0 g, 68 mmol), 4-isopropoxyphenylboronic acid (13.4 g, 75 mmol) and copper (II) acetate (5.0 g, 27 mmol) and the reaction mixture was stirred at room temperature for 16 hours. The crude mixture was then treated with 1M HCl (3×350 mL), followed by aqueous saturated NaHCO3 solution (3×350 mL). The resulting organic faction was concentrated in vacuo and the residue was dissolved in CH2Cl2, dried over MgSO4, concentrated in vacuo, and re-suspended in CH2Cl2. The suspension was filtered and the filtrate was concentrated in vacuo. The crude product was recrystallized from a mixture of toluene/hexane (3:1), giving the desired product (7.6 g, 27 mmol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07166635B2
출처 데이터셋uspto-grants-2007_01
ORD IDord-762a474162cf4bfc98323d7edd6e7cb5
출처 메모uspto-grants-2007_01