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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028368Generated: November 1, 2026

Acetanilide → HCID 11229794, compound

https://huagongshe.com/reaction/1028368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetanilideHCID 904—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Bromo-3-nitrotolueneHCID 231828—
CatalystIronHCID 23925—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTolueneHCID 1140—
ProductHCID 11229794HCID 1122979441.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

A reaction tube containing 2-Bromo-3-nitrotoluene (108 mg, 0.5 mmol), N-phenylacetamide (81 mg, 0.6 mmol) and trans-1,2-cyclohexanodiamine (6 μL, 0.05 mmol), potassium phosphate (212 mg, 1 mmol), copper(I) iodide (9.5 mg, 0.05 mmol) in dry toluene (3 mL) was purged with dry argon for 3 min. Then the mixture was heated at 100° C. for 18 h. After cooling, the reaction was hydrolyzed with 3 mL of water and filtered through a Varian cartridge Chem Elut 12198007, rinsing with ethyl acetate. The crude mixture was dissolved in 10 mL of glacial acetic acid and refluxed for 30 min in the presence of iron powder (279 mg, 5 mmol). The acid was removed under reduced pressure and the residue was suspended in saturated sodium bicarbonate solution and extracted with ethyl acetate. The obtained crude was purified by preparative HPLC, affording the title compound as a pale yellow solid (46 mg, 41%). mp 107-109° C. NMR (DMSO) δ 1.83 (s, 3 H), 2.34 (s, 3 H), 7.02 (d, J=7.8 Hz, 1 H), 7.22 (t, J=7.8 Hz, 1 H), 7.53 (d, J=7.8 Hz, 1 H), 7.55-7.63 (m, 5 H); 13C NMR δ 13.3, 17.1, 114.8, 121.7, 123.0, 125.5, 128.6, 129.4, 129.9, 136.0, 144.5, 151.2, 157.2. HRMS (FAB): cal. for C15H15N2 [M+H+]: 223.1235; found: 223.1231.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735586B2
Source datasetuspto-grants-2014_05
ORD IDord-4e264417b609469b8d6bf3526c44260b
Source noteuspto-grants-2014_05