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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709015Generated: October 29, 2026

Iodoethane → HCID 86681545, compound

https://huagongshe.com/reaction/709015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantHexylcaineHCID 10770—
ReactantPotassium CarbonateHCID 11430—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 86681545HCID 86681545—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred solution of benzoic acid 2-cyclohexylamino-1-methyl-ethyl ester (1.0 g, 3.8 mmol) in DCE (20 mL) were added successively K2CO3 (2.11 g, 15.2 mmol) and ethyl iodide (1.8 mL, 22 mmol). The resulting mixture was heated at 50° C. for 16 hours in a sealed tube. Ethyl iodide (1.8 mL) was again added and the reaction mixture heated at 60° C. for another 24 hours. The reaction mixture was filtered and washed 5% methanol-DCM. The filtrate was concentrated and the crude material was purified by Combiflash® chromatography eluting with 6-7% methanol/DCM to provide 1-(cyclohexyl(ethyl)amino)propan-2-yl benzoate. Yield: 1.04 g (94.70%). 1H NMR (DMSO-d5) δ 7.95 (d, J=7 Hz, 2H), 7.64 (t, J=7 Hz, 1H), 7.52 (t, J=8 Hz, 2H), 5.08-5.04 (m, 1H), 2.68-2.62 (m, 1H), 2.55-2.40 (m, 4H), 1.70-1.53 (m, 5H), 1.26 (d, J=6 Hz, 3H), 1.19-1.07 (m, 5H), 0.93 (t, J=7 Hz, 3H). LCMS: m/z=290.4 [M+H], RT=3.93 min, (Column: Y, Program: P1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09180115B2
Source datasetuspto-grants-2015_11
ORD IDord-baa4c64e630f494580f414467eb26f15
Source noteuspto-grants-2015_11