HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-(2-Ethyl-6-methylphenyl)-1-methyl-2-thioxo-imidazolidin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Ethyl-6-methylphenyl isothiocyanate | HCID 144188 | — |
| Reactant | Ethyl N-methylaminoacetate hydrochloride | HCID 171173 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-(2-Ethyl-6-methylphenyl)-1-methyl-2-thioxo-imidazolidin-4-one | HCID 85701470 | 60% |
Reaction Steps
The title compound was prepared by the procedure described in Example 1 using 8.9 g of 2-ethyl-6-methylphenyl-isothiocyanate, 7.68 g of sarcosine ethyl ester hydrochloride, 12.5 g of triethyl amine, and 250 mL of chloroform. Crystallization from diethyl ether afforded the title compound (7.45 g) as a peach solid, m.p. 106°-108° C. Anal. Calcd. for C13H16N2O S: C, 62.87; H, 6.49; N, 11.28. Found: C, 62.52; H, 6.61; N, 11.29. Mass spectrum (+ESI, [M+H]+) m/z 269/271.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05554607 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-a74ce4bf1f4e4ff389807055323a3b81 |
| Source note | uspto-grants-1996_09 |