HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium cyanoborohydride → 5-(3-Thienyl)indoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 5-(Thiophen-3-yl)-1H-indole | HCID 14973227 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-(3-Thienyl)indoline | HCID 20099954 | 100% |
Reaction Steps
5-(3-Thienyl)indole D40 was reduced in the usual way with sodium cyano borohydride in glacial acetic acid to give the title compound (D41) (1.0 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05834494 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-897ff97657e549949f21d17da38e6886 |
| Source note | uspto-grants-1998_11 |