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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748736Generated: October 31, 2026

Potassium Phosphate, Tribasic → 4-Chloro-2-cyclopropylbenzaldehyde

https://huagongshe.com/reaction/1748736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Bromo-4-chlorobenzaldehydeHCID 13154710—
Reactant2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenylHCID 16217985—
ReactantPotassium cyclopropyltrifluoroborateHCID 23697338—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product4-Chloro-2-cyclopropylbenzaldehydeHCID 5697224841.9%

Reaction Steps

To a degassed mixture of toluene (60 mL) and water (9 mL) was added potassium cyclopropyl-trifluoroborate (0.91 g, 6.2 mmol) and tribasic potassium phosphate (6.37 g, 30 mmol). The resulting mixture was stirred for 15 min at rt, thereafter, 2-bromo-4-chlorobenzaldehyde (1.50 g, 6.84 mmol, WO2006044454), palladium(II) acetate (0.11 g, 0.5 mmol) and 2-dicyclohexylphosphino-2′,6′-diisopropoxybiphenyl (0.48 g, 1.0 mmol) were added and the mixture was heated under reflux, overnight. After cooling to rt, water (50 mL) and ethyl acetate (50 mL) were added and the layers were separated. The organic layer was washed with brine (20 mL), dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by column chromatography (SiO2, DCM/hexanes 1:3) to give 4-chloro-2-cyclopropyl-benzaldehyde (0.48 g, 2.6 mmol, 39%) as a colorless semi solid: 1H-NMR (CDCl3, Bruker 400 MHz) δ 0.80 (2 H, m), 1.08-1.17 (2 H, m), 2.58 (1 H, m), 7.10 (1 H, d, J=2 Hz), 7.29 (1 H, dd, J=8 Hz, 2 Hz), 7.75 (1 H, d, J=8 Hz), 10.6 (1 H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150592B2
Source datasetuspto-grants-2015_10
ORD IDord-912ba6cacb634541b1c015fc7b546a0e
Source noteuspto-grants-2015_10