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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dodecane | HCID 8182 | — |
| Reactant | Hexamethylphosphorous triamide | HCID 15355 | — |
| Reactant | N-Methylformamide | HCID 31254 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 1-Iodo-3,5-dimethylbenzene | HCID 140924 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(3,5-dimethylphenyl)-N-methylformamide | HCID 9855564 | 76% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07115784B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-a086cf3c3a7c445b815a3c5fec91c8e9 |
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| Source note | uspto-grants-2006_10 |
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