Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906154Generated: October 27, 2026

Cesium carbonate → (R)-methyl 5-(sec-butylamino)-4-cyano-2-methylbenzoate

https://huagongshe.com/reaction/906154

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant(R)-sec-butylamineHCID 2724537—
ReactantMethyl 4-cyano-5-iodo-2-methylbenzoateHCID 67402433—
ReactantBis(diphenylphosphino)xantheneHCID 86631950—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
Product(R)-methyl 5-(sec-butylamino)-4-cyano-2-methylbenzoateHCID 6740484973.4%

Reaction Conditions

Temperature95 °C

Reaction Steps

To a solution of methyl 4-cyano-5-iodo-2-methylbenzoate (500 mg, 1.66 mmol) in 1,4-dioxane (25 mL) was added 9,9-dimethyl-4,5-(bis(diphenylphosphino)xanthene (96 mg, 0.166 mmol), tris(dibenzylideneacetone)-dipalladium (76 mg, 0.083 mmol), cesium carbonate (1.08 g, 3.32 mmol) and (R)-butan-2-amine (506 μL, 4.98 mmol). The reaction mixture was heated to 95° C. and stirred for 16 h, at which time it was cooled to room temperature. The heterogeneous mixture was filtered through a bed of celite, and the filter cake rinsed with ethyl acetate. The filtrate was concentrated, and the residue was purified by flash chromatography (100% hexanes to 5% ethyl acetate in hexanes) to afford (R)-methyl 5-(sec-butylamino)-4-cyano-2-methylbenzoate (300 mg, 73%) as a bright yellow oil. MS (EI) for C14H18N2O2: 247 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012956B2
Source datasetuspto-grants-2011_09
ORD IDord-56f4bd5e5abc4c9cb6205e213034de88
Source noteuspto-grants-2011_09