돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16620생성일: 2026년 10월 23일

Isatin → 3-Hydroxy-3-phenyl-1,3-dihydroindol-2-one

https://huagongshe.com/ko/reaction/16620

반응식

참여 물질

역할이름HCID투입량
반응물IsatinHCID 7054—
반응물3-(5-tert-Butyl-2-hydroxy-phenyl)-3-phenyl-1,3-dihydro-indol-2-oneHCID 10406055—
반응물HCID 178418255HCID 178418255—
용매TetrahydrofuranHCID 8028—
생성물3-Hydroxy-3-phenyl-1,3-dihydroindol-2-oneHCID 1580690%

반응 단계

As another non-limiting example, 3-(5-tert-butyl-2-hydroxy-phenyl)-3-phenyl-1,3-dihydro-indol-2-one (compound 1181) was synthesized by adding dropwise a 1M solution of phenylmagnesiumbromide (0.33 mole) to isatin (15 g, 0.1 mole) in 60 mL THF at 0° C. The resulting mixture was allowed to warm to room temperature and let stir at room temperature for 12 hours. The reaction mixture was quenched with a saturated solution of NH4Cl (100 mL) and diluted with 100 mL of dichloromethane. The layers were separated, the organic layer was washed with water followed by brine, dried over Na2SO4, and filtered. The filtrate was concentrated in vacuo to yield 20.1 g (90 %) of 3-hydroxy-3-phenyl-1,3-dihydro-indol-2-one. A mixture of the above solid (2.5 g, 10 mmole), p-t-Bu-phenol (1.5 g, 10 mmol), p-toluenesulfonic acid (3 g) in 40 mL dichloroethane, was heated to 95° C. for six hours. The mixture was cooled and filtered. The filtrate was concentrated in vacuo to yield 2.4 g (66%) of the desired product (compound 1181).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737172B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-e729176a080341c79ac7b95818a36bac
출처 메모uspto-grants-2010_06