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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243124Generated: October 25, 2026

Dodecane → N-(3,5-dimethylphenyl)-N-methylformamide

https://huagongshe.com/reaction/1243124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDodecaneHCID 8182—
ReactantHexamethylphosphorous triamideHCID 15355—
ReactantN-MethylformamideHCID 31254—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1-Iodo-3,5-dimethylbenzeneHCID 140924—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductN-(3,5-dimethylphenyl)-N-methylformamideHCID 985556476%

Reaction Conditions

Temperature110 °C

Reaction Steps

A Schlenk tube was charged with CuI (9.6 mg, 0.050 mmol, 5.0 mol %), K3PO4 (430 mg, 2.03 mmol), evacuated, backfilled with Ar. Hexamethylphosphorous triamide (18.5 μL, 0.102 mmol, 10 mol %) 5-iodo-m-xylene (145 μL, 1.00 mmol), N-methylformamide (72 μL, 1.23 mmol), and toluene (1.0 mL) were added under Ar. The Schlenk tube was sealed with a Teflon valve and the reaction mixture was stirred at 110° C. for 24 h. The suspension was allowed to reach room temperature. Dodecane (internal GC standard, 230 μL) and ethyl acetate (2 mL) were added. A 0.1 mL sample of the supernatant solution was diluted with ethyl acetate (1 mL) and analyzed by GC to provide 76% yield of N-(3,5-dimethylphenyl)-N-methylformamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115784B2
Source datasetuspto-grants-2006_10
ORD IDord-a086cf3c3a7c445b815a3c5fec91c8e9
Source noteuspto-grants-2006_10