HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 68001651, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 86687800 | HCID 86687800 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 68001651 | HCID 68001651 | 69% |
Reaction Steps
To a suspension of the aldehyde obtained above (850 mg, 5.1 mmol) in MeOH (25 mL) at 0° C. was added sodium tetrahydroborate (190 mg, 5.10 mmol) and the reaction mixture warmed to RT for 2 hr and then quenched by the addition of hydrochloric acid (1 M, 5.0 mL) The mixture was diluted with sat aq. NaHCO3 (40 mL) and was extracted with DCM (80 mL, 6×100 mL). The combined organic extracts were dried and evaporated in vacuo to afford (2-amino-3-nitropyridin-4-yl)methanol as an orange solid (630 mg, 69%); Rt 0.40 min (Method 2); m/z 170 (M+H)+, (ES+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08933228B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-1cfc0b70379a4fbeb6329d131a861329 |
| Source note | uspto-grants-2015_01 |