HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 59395108, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 59395098 | HCID 59395098 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 59395108 | HCID 59395108 | 100.7% |
Reaction Steps
A 156 mg portion of sodium borohydride was added to a 10 ml methanol suspension of 280 mg N-(diaminomethylene)-8-oxo-8H-indeno[2,1-b]thiophene-6-carboxamide, followed by stirring at room temperature for 30 minutes. After evaporation of the solvent, the solid precipitated by adding water was purified by Chromatorex (DMF/chloroform) to obtain 284 mg of N-(diaminomethylene)-8-hydroxy-8H-indeno[2,1-b]thiophene-6-carboxamide as a pale green solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08076348B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-e181345536bb4a6b8efffa7833ffd9aa |
| Source note | uspto-grants-2011_12 |