HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040745Generated: October 31, 2026
Dichloromethane → 7-Fluoro-3,4,4a,5-tetrahydro-2H-indeno[1,2-b]pyridine
https://huagongshe.com/reaction/2040745
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Bromopropylamine | HCID 78702 | — |
| Reactant | 5-Fluoro-1-indanone | HCID 136537 | — |
| Catalyst | Diamminetetrachlorotitanate(IV) | HCID 160960 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-Fluoro-3,4,4a,5-tetrahydro-2H-indeno[1,2-b]pyridine | HCID 14075057 | — |
Reaction Steps
3-Bromopropylamine (4.7 g. 21.7 mmole) and 5-Fluoro-1-indanone (2.5 g, 16.7 mmole) were dissolved in 50 ml DMF and the reaction was cooled to 0° C. Triethylamine (13.5 g, 133 mmole) was added. 20 ml DCM was also added to help with the stirring. Titanium chloride (1M in DCM, 15 ml) was then added and the ice bath was removed. The reaction was stirred at room temperature overnight. 200 ml ether was added and the reaction was filtered though a Celite cake. The filtrate was concentrated to dryness under vacuum. The residue was dissolved in 200 ml ether and washed with brine (2×200 ml). The organic layer was dried over sodium sulfate and concentrated to dryness. 2.6 g Black oil was obtained and it was used in next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08580956B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-36384d1985414c868f5e2a91fc2bb6bb |
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| Source note | uspto-grants-2013_11 |
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