HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-Imidazolidinone, 3-(diphenylmethyl)-1-methyl-2-thioxo-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl N-methylaminoacetate hydrochloride | HCID 171173 | — |
| Reactant | Benzhydryl isothiocyanate | HCID 520742 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-Imidazolidinone, 3-(diphenylmethyl)-1-methyl-2-thioxo- | HCID 11150625 | 50% |
Reaction Steps
A mixture of sarcosine ethyl ester hydrochloride (7.68 g), benzhydryl-isothiocyanate (11.25 g), triethyl amine (12 g) and chloroform (200 mL) was heated at reflux for 5 hours. The mixture was cooled to ambient temperature, washed with 1N HCl (2×200 mL), then with water (200 mL) The organic phase was evaporated to dryness. The residue was crystallized from ethanol to give the title compound (7.40 g) as an off-white solid, m.p. 139°-141° C. Anal. Calcd. for C17H16N2O S: C, 68.89; H, 5.44; N, 9.45. Found: C, 68.92; H, 5.43; N, 9.58. Mass spectrum (EI, M.+) m/z 296.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05783707 |
| Source dataset | uspto-grants-1998_07 |
| ORD ID | ord-a0cec222b0794bc1a1dab894d14b4bf6 |
| Source note | uspto-grants-1998_07 |