HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium borohydride → HCID 59395049, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | HCID 59394968 | HCID 59394968 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59395049 | HCID 59395049 | 69% |
Reaction Steps
Ethyl 5-(5-methyl-2-nitro-phenyl)-1,2,4-oxadiazole-3-carboxylate (60 mg, 0.22 mmol) was dissolved in ethanol (3 mL) and treated with lithium borohydride (9 mg, 0.43 mmol) at room temperature. The mixture was stirred for 1 h, then quenched with saturated NH4Cl and extracted into dichloromethane. The organic layer was washed with brine, dried over Na2SO4, filtered and concentrated in vacuo to provide (5-(5-methyl-2-nitrophenyl)-1,2,4-oxadiazol-3-yl)methanol (35 mg, 69% yield). LC/MS m/z 236.0 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08633189B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-b1c7a5eef0954e939429410006ba6d30 |
| Source note | uspto-grants-2014_01 |