HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 69353261, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-Bromo-2-methoxy-3-nitrobenzaldehyde | HCID 21093747 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69353261 | HCID 69353261 | 82.3% |
Reaction Steps
Sodium borohydride (4 g) was added in portions to a stirring solution of crude 5-bromo-2-methoxy-3-nitrobenzaldehyde (20.5 g) in methanol (350 mL) and tetrahydrofuran (150 mL) at 0° C. After 1 h, the methanol was removed in vacuo. The residue was treated with cold water (150 mL) and extracted with diethyl ether (2×150 mL). The combined organic layer was evaporated in vacuo to give a crude oil. Silica gel chromatography eluting with ethyl acetate in petroleum ether (10–40%) gave the title compound (17 g) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07214674B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-1f72f1a800ac48aeb6e9e41e2e9b490f |
| Source note | uspto-grants-2007_05 |