HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 5-Chloro-1-(4-fluorophenyl)-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-Chloro-1-(4-fluorophenyl)-1H-indol-3-yl acetate | HCID 10924714 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Chloro-1-(4-fluorophenyl)-1H-indole | HCID 10236188 | — |
Reaction Steps
1-(4-flourophenyl)-3-acetoxy-5-chloroindole (100.0 g, 0.33 mol) was dissolved in 1000 mL EtOH. During the next hour sodium borohydride pellets (18.7 g, 1.5 eq.) were added batchwise at reflux. The reaction mixture was stirred over night at reflux and cooled to room temperature. Concentrated HCl (appr. 50 mL until pH 1) was added and the reaction mixture was stirred at room temperature for 1 hour. 200 mL demineralized water was added, and the resulting suspension was filtrated. The filter cake was washed with further 50 mL water and 10 mL EtOH. The product was dried over night in vacuum at 50° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06335463B1 |
| Source dataset | uspto-grants-2002_01 |
| ORD ID | ord-e395ac259c25496d9df308b94b7242bd |
| Source note | uspto-grants-2002_01 |