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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417730Generated: November 3, 2026

Iodoethane → 3-(2-Chloro-6-methylphenyl)-2-ethylsulfanyl-3,5-dihydroimidazol-4-one

https://huagongshe.com/reaction/1417730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
Reactant2-[3-(2-Chloro-6-methylphenyl)-thioureido]-acetamideHCID 54394060—
SolventHydrochloric AcidHCID 313—
Product3-(2-Chloro-6-methylphenyl)-2-ethylsulfanyl-3,5-dihydroimidazol-4-oneHCID 44295822—

Reaction Steps

The title compound was prepared by the procedure described in Example 6 using 12.9 g of 2-[3-(2-chloro-6-methylphenyl)-thioureido]-acetamide, and 18.0 g of ethyl iodide. The hydrochloride salt was prepared in ethereal hydrogen chloride. Crystallization from ethyl acetate afforded the title compound as the mono-hydrochloride as a light yellow solid (4.9 g), m.p. 152°-154° C. (dec.). Anal. Calcd. for. C12H13Cl N2O S . HCl: C, 47.22; H, 4.62; N, 9.18. Found: C, 46.99; H, 4.60; N, 9.16. Mass spectrum (+FAB, [M+H]+) m/z 269/271. 1H-NMR (DMSO-d6 ; 400 MHz) δ8.28 (broad s, 2 H), 7.51 (m, 1 H), 7.44 (t, 1 H), 7.39 (m, 1 H), 4.51 (q, 2 H), 3.12 (q, 2 H), 2.17 (s, 3 H), and 1.27 ppm (t, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05877324
Source datasetuspto-grants-1999_03
ORD IDord-08c68caee35145ceb4913bfa61450027
Source noteuspto-grants-1999_03