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 | — |
| Product | 5-Bromoindoline | HCID 3411566 | — |
Reaction Steps
NaBH3CN (19.3 g, 0.3061 mol) was added in 3 portions to a cooled (15° C.) solution of 5-bromoindole (20 g, 0.10 mol) in glacial acetic acid (500 mL) and stirred for 2 h at this same temperature. The reaction mixture was quenched with water, cooled and basified with a sodium hydroxide pellet. It was then extracted with diethyl ether. The organic layer was washed with water and brine, dried over sodium sulfate, concentrated and purified by column chromatography over silica gel to give the sub-title compound as a pale yellow solid. Yield: 20 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07648985B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-15ed5aa6e9724c6ebe7e3e4c39d1e8a5 |
| Source note | uspto-grants-2010_01 |