HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499234Generated: November 1, 2026
3-Bromoanisole → N-Cyclopropyl-3-methoxyaniline
https://huagongshe.com/reaction/499234
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Bromoanisole | HCID 16971 | — |
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-Cyclopropyl-3-methoxyaniline | HCID 45091015 | — |
Reaction Steps
To a high-pressure tube was added 3-bromoanisole(0.250 mL, 2 mmol), cyclopropylamine (0.225 mL, 3.2 mmol), sodium t-butoxide (0.29 g, 3.0 mmol), (+/−) BINAP (0.04 g, 0.06 mmol), and Pd2(dba)3 (0.010 g, 0.01 mmol). This mixture was suspended in 4 mL anhydrous toluene. The tube was flushed with dry nitrogen gas, then capped and wrapped in aluminum foil. The reaction mixture was stirred and heated to 80° C. overnight, then allowed to cool, and the reaction vessel was opened. The mixture was diluted with diethyl ether, filtered through Celite, and the filtrate was concentrated to a yellow oil. LC/MS analysis showed one peak with the correct mass, and due to the limited stability of the material, it was carried through without further purification. FIA MS 164 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07767680B2 |
|---|
| Source dataset | uspto-grants-2010_08 |
|---|
| ORD ID | ord-6bd01bec80b34901b245ad4efea01bd4 |
|---|
| Source note | uspto-grants-2010_08 |
|---|