Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417738Generated: November 2, 2026

Iodoethane → HCID 44295501, compound

https://huagongshe.com/reaction/1417738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantHCID 54019612HCID 54019612—
SolventEthanolHCID 702—
ProductHCID 44295501HCID 4429550180.6%

Reaction Steps

A mixture of 2-[3-(3-chloro-4-methylphenyl)-thioureido]-acetamide (10.0 g), ethyl iodide (17.5 g), and ethanol (200 mL) was heated at reflux for 2.5 hours. The solvent was evaporated. The residue was dissolved in ethyl acetate (500 mL) and water (500 mL). The organic phase was washed with water (2×300 mL). The organic phase was extracted with 2N HCl (2×500 mL). The acid extract was neutralized with solid sodium bicarbonate and extracted with ethyl acetate. The organic phase was washed with water, dried over anhydrous Na2SO4 then evaporated to dryness. The residue was stirred in diethyl ether and filtered to give the title compound (8.4 g) as a white solid, m.p. 133°-135° C. Anal. Calcd. for. C12H13Cl N2O S: C, 53.63; H, 4.88; N,10.42. Found: C, 53.66; H, 4.78; N, 10.39. Mass spectrum (EI, M.+) m/z 268/270. 1H-NMR (DMSO-d6 ; 400 MHz) δ7.47 (d, 1 H), 7.43 (d, 1 H), 7.20 (dd, 1 H), 4.29 (s, 2 H), 3.07 (q, 2 H), 2.36 (s, 3 H), and 1.28 ppm (t, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05877324
Source datasetuspto-grants-1999_03
ORD IDord-d6bc7b76e064486abb79e6803db0ec21
Source noteuspto-grants-1999_03