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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465155Generated: November 1, 2026

Lithium borohydride → HCID 59395049, compound

https://huagongshe.com/reaction/1465155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium borohydrideHCID 4148881—
ReactantHCID 59394968HCID 59394968—
SolventEthanolHCID 702—
ProductHCID 59395049HCID 5939504969%

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, 0.4 mmol) at room temperature. The mixture was stirred for 1 h then quenched with saturated ammonium chloride 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999976B2
Source datasetuspto-grants-2015_04
ORD IDord-9c7a40435df84034af639cf0decc376d
Source noteuspto-grants-2015_04