HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-(2-Chloro-6-methylphenyl)-1-methyl-2-thioxo-imidazolidin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl N-methylaminoacetate hydrochloride | HCID 171173 | — |
| Reactant | 2-Chloro-6-Methylphenyl Isothiocyanate | HCID 3731725 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-(2-Chloro-6-methylphenyl)-1-methyl-2-thioxo-imidazolidin-4-one | HCID 11425342 | 55.7% |
Reaction Steps
The title compound was prepared by the procedure described in Example 1 using 9.2 g of 2-chloro-6-methylphenyl-isothiocyanate, 7.68 g of sarcosine ethyl ester hydrochloride, 12 g of triethyl amine, and 200 mL of chloroform. Crystallization from ethanol afforded the title compound (7.1 g) as an orange solid (7.1 g), m.p. 142°-145° C. Anal. Calcd. for. C11H11N2O S: C, 51.87; H, 4.35; N,11.00. Found: C, 51.96; H, 4.26; N, 10.97. Mass spectrum (El, M.+) m/z 254.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05554607 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-fac5c77daf104020a734746a13c2f567 |
| Source note | uspto-grants-1996_09 |