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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 872022Generated: October 30, 2026

Potassium Phosphate, Tribasic → HCID 59494673, compound

https://huagongshe.com/reaction/872022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTrimethylboroxineHCID 574072—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
ReactantHCID 59494587HCID 59494587—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 59494673HCID 59494673—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of tert-butyl [2-bromo-4-methoxy-5-(3-methoxypropoxy)benzyl]cyclopropylcarbamate (200 mg), trimethylboroxin (94 μL), tris(dibenzylideneacetone)dipalladium (8.2 mg), 2-dicyclohexylphosphino-2′,4′,6′-triisopropyl-1,1′-biphenyl (X-phos) (21.5 mg) and potassium phosphate (191 mg) in dioxane (7.0 ml) was stirred under argon atmosphere at 100° C. for 23 hours. After being stand to cool, water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over magnesium sulfate and concentrated in vacuo. The resulted residue was purified with a NH-silica gel column chromatography (eluting solvent: n-hexane/ethyl acetate=10/1 to 3/1) to give tert-butyl cyclopropyl[4-methoxy-5-(3-methoxypropoxy)-2-methylbenzyl]carbamate (103 mg) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975252B2
Source datasetuspto-grants-2015_03
ORD IDord-d75a15f42bc045caad1b03e617607f93
Source noteuspto-grants-2015_03