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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275244Generated: November 1, 2026

Cyclopropanecarboxaldehyde → HCID 22993501, compound

https://huagongshe.com/reaction/1275244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropanecarboxaldehydeHCID 123114—
ReactantHCID 69523584HCID 69523584—
ReactantHCID 178418306HCID 178418306—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22993501HCID 22993501—

Reaction Conditions

Temperature-78 °C

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 (1.7M, 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06159990
Source datasetuspto-grants-2000_12
ORD IDord-d37170c69e7a4dce8b91bb6bb00b3430
Source noteuspto-grants-2000_12