HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → HCID 12031585, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | HCID 53927476 | HCID 53927476 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 12031585 | HCID 12031585 | 41.5% |
Reaction Steps
A mixture of 2-(3-phenyl-thioureido)-acetamide (7.1 g), ethyl iodide (18.0 g), and ethanol (300 mL) was heated at reflux for 2 hours. The solvent was evaporated. The residue was dissolved in chloroform (300 mL) and water (300 mL). The organic phase was washed with water, dried over anhydrous MgSO4, then evaporated to dryness. The residue was crystallized from ethyl acetate/hexane to give the title compound (3.1 g), m.p. 79°-81° C. Anal. Calcd. for. C11H12N2O S: C, 59.97; H, 5.49; N, 12.72. Found: C, 59.67; H, 5.35; N, 12.70. Mass spectrum (El, M.+) m/z 220. 1H-NMR (DMSO-d6 ; 400 MHz) δ7.43-7.52 (m, 3H), 7.28-7.31 (m, 2H), 4.32 (s, 2H), 3.07 (q, 2H), and 1.27 ppm (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05599829 |
| Source dataset | uspto-grants-1997_02 |
| ORD ID | ord-640c7afb42a24b45938fb963f885a961 |
| Source note | uspto-grants-1997_02 |