HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Bromoindole → 5-Bromoindoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Bromoindole | HCID 24905 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Bromoindoline | HCID 3411566 | 71% |
Reaction Steps
To 5-Bromo-1H-indole (2.5 g, 12.82 mmol) in acetic acid (10.0 mL), NaCNBH3 (2.38 g, 38.46 mmol) was added portion wise at 10° C. over the period of 20 min After that the reaction mixture was stirred at ambient temperature for 3 h. The reaction mixture was diluted with water and extracted with diethyl ether. The organic layer was washed with saturated NaHCO3, water and brine solution. The combined ether layer was dried over anhydrous Na2SO4 and concentrated under reduced pressure to afford title compound as a pale yellow semi-solid (1.8 g, 71%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09211281B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-218536f925c943529bb05939931b6bf3 |
| Source note | uspto-grants-2015_12 |