Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropylamine | HCID 6363 | — |
| Reactant | 2-Cyano-3-fluorobiphenyl | HCID 23509652 | — |
| Product | HCID 23509647 | HCID 23509647 | — |
Reaction Steps
The product of example 1a above, 2-fluoro-6-phenylbenzonitrile, (0.12 g, 0.61 mmol), and isopropylamine (3 mL) were combined in a sealed tube that had been flushed with argon. The tube was heated in an oil bath to 95° C. for 7 days. The excess isopropylamine was evaporated, .and the residue was flash chromatographed on silica gel eluted with 0-3% ethyl acetate in hexane, and then crystallized from hexane to give the title product as a white crystalline product. ES (+) MS m/e=237 (MH+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06759410B1 |
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| Source dataset | uspto-grants-2004_07 |
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| ORD ID | ord-43e062be610b4d17b9a5fb52443be60e |
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| Source note | uspto-grants-2004_07 |
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