HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 178445669, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4,6-Dichloropyrimidine | HCID 70943 | — |
| Reactant | HCID 178445676 | HCID 178445676 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178445669 | HCID 178445669 | — |
Reaction Steps
58.6 g (0.39 mol) of 4,6-dichloropyrimidine were placed in 400 ml of toluene, and a mixture of 61.0 g (0.39 mol) of cis-4-tert-butylcyclohexylamine and 50.0 g (0.50 mol) of triethylamine in 100 ml of toluene was added dropwise at from 70° to 80° C. The mixture was subsequently stirred at reflux for 4 hours. After cooling, it was extracted by stirring with water, the organic phase was dried and concentrated, to give a colorless oil which crystallized after trituration with petroleum ether. Filtration with suction left 70.5 g (67.0% of theory) of colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05852023 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-86925259218146fc833252ccebbb8e15 |
| Source note | uspto-grants-1998_12 |