HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 68488240, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 68490381 | HCID 68490381 | — |
| Catalyst | Water | HCID 962 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 68488240 | HCID 68488240 | — |
Reaction Steps
To a 0° C. solution of methyl 5-{[5-(4-acetylphenyl)-6-chloro-1H-benzimidazol-2-yl]oxy}-2-methylbenzoate (50 mg, 0.115 mmol) in MeOH (2 mL) was added NaBH4 (6.5 mg, 0.172 mmol). The mixture was warmed to rt and stirred for 15 min. Water (5-6 drops) was added and the mixture was concentrated. The residue was partitioned between Et2O and water. The aqueous phase was extracted with Et2O. The combined ethereal extracts were washed with brine, dried (MgSO4), filtered, and concentrated to afford the desired product, which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08394969B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-06017660a62c4dabb6db8de89ffdd197 |
| Source note | uspto-grants-2013_03 |