HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 22918594, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Chloro-6-isothiocyanatotoluene | HCID 90021 | — |
| Reactant | HCID 22918592 | HCID 22918592 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22918594 | HCID 22918594 | 26.6% |
Reaction Steps
A mixture of ethyl N-propargylaminoacetate (10.0 g), 4-chloro-2-methylphenylisothiocyanate (12.9 g), triethylamine (7.1 g), and methylene chloride (150 mL) was heated at reflux for 3 hours. The reaction mixture was cooled to ambient temperature, washed with 1 N HCl (100 mL), then with water. The organic layer was dried over anhydrous magnesium sulfate, then evaporated to dryness. The residual oil was triturated with hexane. The solid was collected by filtration. Recrystallization from Hexane-EtOAc afford the title compound (5.2 g) as yellow solid, m.p. 99°-102° C. Anal. Calcd. for. C13H11N2O Cl S: C, 56.01; H, 3.98; N, 10.05. Found: C, 55.61; H, 3.83; N, 10.0. Mass spectrum (EI, M.+) m/z 278.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05554607 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-c3ea7bf6057a49029704417e469d422c |
| Source note | uspto-grants-1996_09 |