HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 1,4-Bis(6-chloropyridin-3-yl)butane-1,4-diol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1,4-Bis(6-chloropyridin-3-yl)butane-1,4-dione | HCID 59617025 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1,4-Bis(6-chloropyridin-3-yl)butane-1,4-diol | HCID 59617171 | 89.2% |
Reaction Steps
The product from Example 207A (2.90 g, 9.38 mmol) and sodium borohydride (0.745 g, 19.70 mmol) were combined in ethanol (94 mL) at 0° C. The mixture was warmed to room temperature and stirred for 6 hours. The solvent was evaporated and the residue was partitioned between ethyl acetate and 1M HCl. The organic layer was washed with water, brine, dried with sodium sulfate, filtered and evaporated to give the title compound (2.62 g, 89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08691938B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-00630051184547e2a0ef5305793e6d11 |
| Source note | uspto-grants-2014_04 |