HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(2-Bromoethyl)indole → Indole, 3-(2-(isoindolin-2-yl)ethyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(2-Bromoethyl)indole | HCID 76924 | — |
| Reactant | Isoindole | HCID 3013853 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Indole, 3-(2-(isoindolin-2-yl)ethyl)- | HCID 39465 | — |
Reaction Steps
A solution of 3-(2-bromo-ethyl)-1H-indole (4.48 g, 20 mmol) and isoindole (4.76 g, 40 mmol) in abs. dioxane (50 ml) was stirred at 80° C. for 6 h. The solvent was then removed i. vac., CHCl3 (100 ml) was added to the residue and the mixture was washed twice with water. The organic phase was dried over Na2SO4 and concentrated i. vac. and the residue which remained was purified by flash chromatography with CHCl3/MeOH (20:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08138187B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-bc4bcb7578264a7e9adcb73371d5f13f |
| Source note | uspto-grants-2012_03 |