HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-(Indan-5-yl)-1-methyl-2-thioxo-imidazolidin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl N-methylaminoacetate hydrochloride | HCID 171173 | — |
| Reactant | 5-isothiocyanato-2,3-dihydro-1H-indene | HCID 2759357 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-(Indan-5-yl)-1-methyl-2-thioxo-imidazolidin-4-one | HCID 11195962 | 73.5% |
Reaction Steps
The title compound was prepared by the procedure described in Example 1 using 7.7 g of indan-5-yl-isothiocyanate, 6.7 g of sarcosine ethyl ester hydrochloride, 12 g of triethyl amine, and 300 mL of chloroform. Crystallization from ethyl acetate afforded the title compound (7.9 g) as a tan solid, m.p. 158-160° C. Anal. Calcd. for C13H14N2O S: C, 63.39; H, 5.73; N,11.37. Found: C, 63.30; H, 5.81; N, 11.31. Mass spectrum (EI, M.+) m/z 246.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05554607 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-e1706389bbe84f19a79645e0c53da8c0 |
| Source note | uspto-grants-1996_09 |