HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → [2-(3-Aminoprop-1-yn-1-yl)-5-chlorophenyl](2-fluorophenyl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | HCID 12878253 | HCID 12878253 | — |
| Solvent | Water | HCID 962 | — |
| Product | [2-(3-Aminoprop-1-yn-1-yl)-5-chlorophenyl](2-fluorophenyl)methanone | HCID 12948270 | — |
Reaction Steps
Method B A mixture of 400 g (0.96 mole) of 1-[4-chloro-2-(2-fluorobenzoyl)phenyl]-3-phthalimidopropyne, 1.3 L of ethanol and 300 ml of 40% aqueous methylamine was stirred at room temperature for 2 hr. Dropwise 2.8 l of water was added, and the resulting precipitate was collected by filtration to give a pale yellow solid, mp 70°-80° C. Recrystallization from ether gave pale yellow prisms, mp 80°-91° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04548750 |
| Source dataset | uspto-grants-1985_10 |
| ORD ID | ord-d4ff219e54044bd7a49c0258c4e75ddc |
| Source note | uspto-grants-1985_10 |