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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179243Generated: October 30, 2026

Benzamide → HCID 86609296, compound

https://huagongshe.com/reaction/2179243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzamideHCID 2331—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant(1E)-1-Iodo-1-hexeneHCID 5362933—
Reactant(1R,2R)-N1,N1-Dimethylcyclohexane-1,2-diamineHCID 11275066—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTolueneHCID 1140—
ProductHCID 86609296HCID 86609296668.6%

Reaction Conditions

Temperature25 °C

Reaction Steps

A 15 mL resealable Schlenk tube was charged with CuI (9.6 mg, 0.0504 mmol, 5.0 mol %), benzamide (145 mg, 1.20 mmol), K3PO4 (430 mg, 2.03 mmol), evacuated and backfilled with argon. trans-N,N-Dimethyl-1,2-cyclohexanediamine (16 μL, 0.102 mmol, 10 mol %), trans-1-iodo-1-hexene (143 μL, 1.00 mmol), and toluene (1.0 mL) were added under argon. The Schlenk tube was sealed with a Teflon valve and the reaction mixture was stirred at 25° C. for 24 h. The resulting light blue suspension was allowed to reach room temperature and then filtered through a 0.5×1 cm pad of silica gel eluting with 10 mL of ethyl acetate. The filtrate was concentrated, the residue was dissolved in 5 mL of dichloromethane and purified by flash chromatography on silica gel (2×15 cm, hexane-ethyl acetate, 15 mL fractions). Fractions 12-19 provided 140 mg (69% yield) of the desired product as white needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067955B2
Source datasetuspto-grants-2015_06
ORD IDord-02d73fd03eea4b25848b8f5275298220
Source noteuspto-grants-2015_06