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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628803Generated: October 30, 2026

P-Chloroacetophenone → HCID 86619548, compound

https://huagongshe.com/reaction/628803

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), Pd2dba3 (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 numberUS09315457B2
Source datasetuspto-grants-2016_04
ORD IDord-4201ee3e0d624c13b27b3dede5b5c4cf
Source noteuspto-grants-2016_04