HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dibromopropane → 5-(3-bromopropyl)oxy-4-propyl-N-(4-chlorophenyl)indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-hydroxy-4-propyl-N-(4-chlorophenyl)indole | HCID 53747016 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | 5-(3-bromopropyl)oxy-4-propyl-N-(4-chlorophenyl)indole | HCID 54446720 | — |
Reaction Steps
To a solution of 5-hydroxy-4-propyl-N-(4-chlorophenyl)indole (Step D; 500 mg, 1.75 mmol) and potassium carbonate (484 mg, 3.50 mmol) in 7 mL of dimethylformamide (DMF) was added 1,3-dibromopropane (1.77 g, 8.75 mmol). The mixture was stirred at ambient temperature for 2 hours and diluted with ethyl acetate and saturated aqueous ammonium chloride. The aqueous phase was extracted with ethyl acetate and the combined organic extracts were washed brine, dried over magnesium sulfate, filtered, concentrated in vacuo, and the crude residue was used as is in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05859051 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-9a8828c43a1749eca064fb2fec71abed |
| Source note | uspto-grants-1999_01 |