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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850714Generated: October 27, 2026

5-Benzyloxy-2-bromotoluene → HCID 70856270, compound

https://huagongshe.com/reaction/1850714

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Benzyloxy-2-bromotolueneHCID 2756639—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
ReactantHCID 178451183HCID 178451183—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 70856270HCID 70856270—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 5-benzyloxy-2-bromotoluene (1 g, 3.61 mmol) in THF (10 ml) was added 2-tert-butoxy-2-oxoethylzinc chloride (18.04 ml, 9.02 mmol). Nitrogen gas bubbled through the mixture for 10 min. then Pd2(dba)3 (0.165 g, 0.180 mmol) and X-PHOS (0.172 g, 0.361 mmol) were added and the resulting mixture heated at 60° C. for 50 min. The mixture was cooled, diluted with ethyl acetate (20 mL), washed with aqueous ammonium chloride (saturated, 1×15 mL), dried over MgSO4, filtered and the solvent evaporated under reduced pressure. The residue was purified by column chromatography on silica gel Biotage 50M, using a gradient eluant of EtOAc/Hexane (0-20%) %) to afford the title compound. LC/MS (m/z): 335(M+Na)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957062B2
Source datasetuspto-grants-2015_02
ORD IDord-60acab5340df473987cd154a2f07e811
Source noteuspto-grants-2015_02