HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allylamine → HCID 22141298, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allylamine | HCID 7853 | — |
| Reactant | Ethyl 3-(chloromethyl)-2-methyl-2-(3-nitrophenyl)cyclopropanecarboxylate | HCID 22141336 | — |
| Product | HCID 22141298 | HCID 22141298 | 100.6% |
Reaction Steps
Ethyl 3-(chloromethyl)-2-methyl-2-(3-nitrophenyl)cyclopropanecarboxylate (Preparation 5, 1 g, 3.36 mmol) in allylamine (1.15 g, 20.1 mmol) was heated in a sealed tube at 150° C. for 16 h. After cooling the reaction mixture was concentrated in vacuo. The residue was dissolved in dichloromethane and washed with saturated aqueous sodium hydrogen carbonate solution. The organic extracts were dried (Na2SO4) and concentrated in vacuo to give the crude product as a yellow oil (0.92 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07049444B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-4447f71cdad64f729f4a30df0f909a2e |
| Source note | uspto-grants-2006_05 |