HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417207Generated: October 25, 2026
Piperidine → Z-6-chloro-3-(3-chloro-2-fluoro-benzylidene)-5-fluoro-1,3-dihydro-indol-2-one
https://huagongshe.com/reaction/417207
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 3-Chloro-2-fluorobenzaldehyde | HCID 736335 | — |
| Reactant | 6-Chloro-5-fluoroindolin-2-one | HCID 9794083 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Z-6-chloro-3-(3-chloro-2-fluoro-benzylidene)-5-fluoro-1,3-dihydro-indol-2-one | HCID 86653933 | 87% |
Reaction Steps
To the mixture of 6-chloro-5-fluoroindolin-2-one (Natrochem) (2.88 g, 15.5 mmol) and 3-chloro-2-fluorobenzaldehyde (3.69 g, 23.3 mmol) (Aldrich) in methanol (140 mL) was added piperidine (3.96 g, 46.6 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, dried to give E/Z-6-chloro-3-(3-chloro-2-fluoro-benzylidene)-5-fluoro-1,3-dihydro-indol-2-one as a yellow solid (Yield 4.4 g, 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088815B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-d6579ea61160444eb895eee759c569ed |
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| Source note | uspto-grants-2012_01 |
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