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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2246882Generated: November 1, 2026

P-Chloroacetophenone → HCID 86619548, compound

https://huagongshe.com/reaction/2246882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-ChloroacetophenoneHCID 7467—
ReactantBinap, (A+-)-HCID 634876—
ReactantTert-butyl 4-bromobenzoateHCID 11334366—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86619548HCID 86619548—

Reaction Steps

A THF solution (200 ml) containing t-butyl 4-bromobenzoate (19.9 g, 77.6 mmol), 4-chloroacetophenone (10 g, 64.7 mmol), Pd2 dba3 (1.19 g, 1.29 mmol), BINAP (1.6 g, 2.58 mmol) and NaOtBu (8.7 g, 90.6 mmol) was refluxed under an argon atmosphere for approximately 5 hours. The solution was concentrated and then partitioned between EtOAc and water. The organic phase was washed with water, brine and dried over Na2SO4. The filtered solution was concentrated and the residue purified by silica gel chromatography using a hexanes/EtOAc gradient to give the title compound. 1H NMR (500 MHz, CDCl3): δ 7.95 (d, J=8.5 Hz, 2H); 7.93 (d, J=8.7 Hz, 2H); 7.43 (d, J=8.3 Hz, 2H); 7.29 (d, J=8.2 Hz, 2H); 4.30 (s, 2H); 1.58 (s, 9H). LC1 4.01 min. (M-tBu+H)=275

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687534B2
Source datasetuspto-grants-2010_03
ORD IDord-4770744d2e0f4e3d87ca028d334907d1
Source noteuspto-grants-2010_03