Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449598Generated: October 31, 2026

Iodoethane → HCID 9795388, compound

https://huagongshe.com/reaction/1449598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantHCID 53995114HCID 53995114—
SolventEthanolHCID 702—
ProductHCID 9795388HCID 979538863.2%

Reaction Steps

A mixture of 2-[3-(5-chloro-2-methylphenyl)-thioureido]-acetamide (25.8 g) and ethyl iodide (32.0 g) was heated at reflux in ethanol (500 mL) for 5 hours. The solvent was evaporated. The residue was dissolved in ethyl acetate (500 mL) and water (300 mL). The organic phase was washed with water, dried over anhydrous MgSO4, then evaporated to dryness. The residue was triturated with diethyl ether and the solid was collected by filtration and dried to give the title compound (17.0 g) as a yellow solid, m.p. 137°-139° C. Anal. Calcd. for. C12H13Cl N2O S: C, 53.63; H, 4.88; N, 10.42. Found: C, 53.58; H, 4.74; N, 10.32. Mass spectrum (EI, M.+) m/z 268/270. 1H-NMR (DMSO-d6 ; 400 MHz) δ7.45-7.49 (m, 1H), 7.40-7.43 (m, 2H), 4.35 (dd, 2H), 3.07 (m, 2H), 2.1 (s, 3H), and 1.28 ppm (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05599829
Source datasetuspto-grants-1997_02
ORD IDord-42defc09e5b145509de93de775f34a40
Source noteuspto-grants-1997_02