HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 16756658, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 16756983 | HCID 16756983 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 16756658 | HCID 16756658 | 103.4% |
Reaction Steps
To a solution of 3-(4-trifluoromethoxyphenyl)-[1,2,4]thiadiazole-5-carboxylic acid ethyl ester (0.11 g, 0.35 mmol) in MeOH (10 ml) was added sodium borohydride (0.022 g, 0.59 mmol) portion wise. The resulting reaction mixture was stirred at room temperature for 2 h. After the completion of the reaction (TLC monitoring), the reaction mass was cooled to 0° C., quenched it with 2 ml of water and concentrated under vacuum. Added water (50 ml) and extracted with ethyl acetate (3×50 ml). The combined organic layer was dried over Na2SO4, filtered and concentrated under vacuum to get the product (0.10 g) that was carried forward to the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08492414B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-8a2786988f884eac8823b1a46ed33357 |
| Source note | uspto-grants-2013_07 |