HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198320Generated: October 31, 2026
Benzene → 4-(4-Pentylcyclohex-1-enyl)-2,3-difluorobenzaldehyde
https://huagongshe.com/reaction/1198320
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1-Piperidinecarboxaldehyde | HCID 17429 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178506716 | HCID 178506716 | — |
| Solvent | Thf tmeda | HCID 86588997 | — |
| Product | 4-(4-Pentylcyclohex-1-enyl)-2,3-difluorobenzaldehyde | HCID 14548486 | — |
Reaction Steps
0.12 mol of N-formylpiperidine in 20 ml of tetrahydrofuran is added to 0.1 mol of 4-(4-pentycyclohex-1-enyl)- 2,3-difluorophenyllithium (prepared from the benzene with n-butyllithium in tetrahydrofuran/tetramethylethylenediamine analogously to Example 7a)) at -70° C. and the mixture is warmed to -20° C. in the course of 1 hour. Acidification and customary working up give the aldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05279764 |
|---|
| Source dataset | uspto-grants-1994_01 |
|---|
| ORD ID | ord-39b4a4d3109b4dc59bc40f943feea4a6 |
|---|
| Source note | uspto-grants-1994_01 |
|---|