Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 417226생성일: 2026년 10월 27일
Piperidine → Z-6-chloro-3-(3-chloro-2-fluoro-benzylidene)-4-fluoro-1,3-dihydro-indol-2-one
https://huagongshe.com/reaction/417226
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Piperidine | HCID 8082 | — |
| 반응물 | 3-Chloro-2-fluorobenzaldehyde | HCID 736335 | — |
| 반응물 | 6-Chloro-4-fluoroindolin-2-one | HCID 66634278 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | Z-6-chloro-3-(3-chloro-2-fluoro-benzylidene)-4-fluoro-1,3-dihydro-indol-2-one | HCID 86653935 | 74.8% |
반응 단계
To the mixture of 6-chloro-4-fluoroindolin-2-one (Natrochem, 85% purity) (1.1 g, 5.0 mmol) and 3-chloro-2-fluorobenzaldehyde (2.4 g, 15 mmol) (Oakwood) in methanol (50 mL) was added piperidine (1.7 g, 20 mmol) (Aldrich) dropwise. The mixture was then heated at 50° C. for 3 h. After cooled to 4° C., the mixture was filtered and resulting precipitate was collected, washed with cold methanol, dried to give the first batch of desired product (1.22 g). The filtrate was concentrated, and the residue was partitioned between ethyl acetate and water. The organic layer was separated, washed with water, brine, dried over MgSO4, and concentrated. The residue was purified by chromatography (20-35% EtOAc in hexanes) to give the second batch of desired product (0.32 g). The two batches were combined to give E/Z-6-chloro-3-(3-chloro-2-fluoro-benzylidene)-4-fluoro-1,3-dihydro-indol-2-one as a yellow solid (Yield 1.54 g, 94%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08088815B2 |
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| 출처 데이터셋 | uspto-grants-2012_01 |
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| ORD ID | ord-1a524774307d45fa97ae122e6351b988 |
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| 출처 메모 | uspto-grants-2012_01 |
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