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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236143Generated: November 3, 2026

Cesium carbonate → methyl N-(t-butyloxycarbonyl)-2-amino-2-[4-(2,6-dimethoxyphenyl)phenyl]acetate

https://huagongshe.com/reaction/2236143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantTricyclohexylphosphineHCID 75806—
Reactant(2,6-Dimethoxyphenyl)boronic acidHCID 2734343—
Reactantmethyl N-(t-butyloxycarbonyl)-2-amino-2-(4-toluenesulfonyloxyphenyl)acetateHCID 86593956—
CatalystBis(1,5-cyclooctadiene)nickelHCID 6433264—
Solvent1,4-DioxaneHCID 31275—
Productmethyl N-(t-butyloxycarbonyl)-2-amino-2-[4-(2,6-dimethoxyphenyl)phenyl]acetateHCID 5896171572.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

Under a nitrogen atmosphere, methyl N-(t-butyloxycarbonyl)-2-amino-2-(4-toluenesulfonyloxyphenyl)acetate (0.44 g, 1.0 mmol), cesium carbonate (0.65 g, 2.0 mmol), tricyclohexylphosphine (0.059 g, 0.2 mmol), bis(1,5-cyclooctadiene)nickel (0.028 g, 0.1 mmol) and 2,6-dimethoxyphenylboronic acid (0.36 g, 2.0 mmol) were mixed in dioxane (1 ml). The reaction mixture was heated to 70° C. and then stirred at the same temperature for 9 hrs. After the reaction was completed, the mixture was left to cool to room temperature and insoluble substances were filtered off. The filtrate was subjected to column chromatography purification to obtain methyl N-(t-butyloxycarbonyl)-2-amino-2-[4-(2,6-dimethoxyphenyl)phenyl]acetate (0.29 g, yield 72%) as pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714157B2
Source datasetuspto-grants-2010_05
ORD IDord-79e0bf1c298c46b89706f37e57838ada
Source noteuspto-grants-2010_05