HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 57772051, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 57772019 | HCID 57772019 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 57772051 | HCID 57772051 | 91.7% |
Reaction Steps
To a solution of 710 mg (1.69 mmol) 2-(4-isopropyl-phenyl)-7-methoxy-1-(2-methoxy-ethyl)-4-trifluoromethyl-1H-benzoimidazole-5-carbaldehyde (example 54c) in 5 ml ethanol, 128 mg (3.38 mmol) NaBH4 are added at 0° C. The mixture is stirred for 30 min at room temperature. Then the reaction mixture is poured on water and extracted (3×) with ethyl acetate. The combined organic layers are washed with water (2×) and brine, dried over MgSO4, filtered and concentrated in vacuo. The residue is crystallized from hexane/EtOAc to afford 655 mg of the title compound as a colorless crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08030497B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-0d7b1fbc0bd24181b490884e06c75804 |
| Source note | uspto-grants-2011_10 |