HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Piperidinecarboxaldehyde → HCID 178444530, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Piperidinecarboxaldehyde | HCID 17429 | — |
| Reactant | hydroxylamine-O-sulfonic acid | HCID 76284 | — |
| Reactant | 2,3-Difluorophenol | HCID 80879 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178444521 | HCID 178444521 | — |
| Solvent | Thf tmeda | HCID 86588997 | — |
| Product | HCID 178444530 | HCID 178444530 | — |
Reaction Steps
0.1 mole of 1-(trans-4pentylcyclohexyl-1-methoxy)-2,3-difluorobenzene (prepared from 2,3-difluorophenol and trans-4-pentylcyclohexylmethyl iodide analogously to Example 4) is deprotonated by means of n-butyllithium in tetrahydrofuran/tetramethylethylenediamine and is formylated by means of N-formylpiperidine. The formyl compound is reacted as in Example 1b) with hydroxylamine-O-sulfonic acid. Working up in the customary manner gives 4-(trans-4-pentylcyclohexylmethoxy)-2,3-difluorobenzonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04925590 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-3e4208f7d13846d1ad9ce7d696e4a73a |
| Source note | uspto-grants-1990_05 |