HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → Indoramin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 18177187 | HCID 18177187 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | (+-)-2-Butanol | HCID 6568 | — |
| Product | Indoramin | HCID 33625 | — |
Reaction Steps
A suspension of 4-benzamido-1-[2-(3-indolyl)ethyl]-pyridinium bromide (10.5g) and sodium borohydride (2.8 g) in sec-butanol (100 ml) was stirred and refluxed for 6 hours. The reaction mixture was cooled to 25° and diluted with aqueous methanol. The product was separated by filtration and washed with aqueous methanol then with water and finally with methanol, and dried to give the crude title compound. This was purified as described in Example 5 to give the title compound mp 203°-5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04162252 |
| Source dataset | uspto-grants-1979_07 |
| ORD ID | ord-349f1a04b1194ffbab9ea60b43cd7da3 |
| Source note | uspto-grants-1979_07 |