HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167728Generated: November 1, 2026
Cyclopropanecarboxaldehyde → HCID 22993501, compound
https://huagongshe.com/reaction/1167728
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclopropanecarboxaldehyde | HCID 123114 | — |
| Reactant | HCID 69523584 | HCID 69523584 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22993501 | HCID 22993501 | — |
Reaction Steps
To a solution of benzhydrylindene-(3,4-difluoro-benzyl)-amine (2.5 g, 8.1 mmol) in 50 mL of dry THF was added tert-butyllithium (1.7 M, 6.2 mL) dropwise and the resulting solution was stirred at −78° C. for 0.5 h. To the solution was added cyclopropanecarboxaldehyde (0.90 ml, 12.0 mmol) in 10 ml of THF and the solution was stirred at −78° C. for 2 h and 25° C. for 1 h. The reaction was quenched by adding 1.0 mL of dilute acetic acid. Reaction mixture was diluted with 100 ml of Et2O and washed with brine. The organic layer was dried over Na2SO4 and concentrated in vacuo, yielding 2-(benzhydryliden-amino)-1-cyclopropyl-2-(3,4-difluoro-phenyl)-ethanol as a yellow oil, which was subjected to the following reaction without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06620815B1 |
|---|
| Source dataset | uspto-grants-2003_09 |
|---|
| ORD ID | ord-8f10bc211c6244aeb7a82136137ccc45 |
|---|
| Source note | uspto-grants-2003_09 |
|---|