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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368046Generated: October 30, 2026

Lithiumtriethylborohydride → HCID 49838698, compound

https://huagongshe.com/reaction/2368046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithiumtriethylborohydrideHCID 23664628—
ReactantHCID 86667491HCID 86667491—
SolventTetrahydrofuranHCID 8028—
ProductHCID 49838698HCID 49838698—

Reaction Steps

Lithium triethylborohydride (1 mol/L in tetrahydrofuran, 4.9 mL) was added to an ice-cold solution of 3-[(4-bromo-phenyl)-cyclopropyl-methyl]-6-(2-methyl-oxiranylmethyl)-6-phenyl-[1,3]oxazinan-2-one (compound processed from diastereomer 2 obtained in Step 3; 1.86 g, ca. 85-90% pure) in tetrahydrofuran (15 mL) at such a rate that the solution temperature remained below 10° C. The resulting solution was stirred in the cooling bath for one more hour and at room temperature for another 3 h. Then, the solution was cooled in an ice bath and the reaction was quenched by the careful addition of water (7 mL). After the addition of hydrochloric acid and ethyl acetate, the organic phase was separated, washed with brine, and dried (MgSO4). The solvent was evaporated to afford the title compound. Yield: 1.45 g (88% of theory); Mass spectrum (ESI+): m/z=458/460 (Br) [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703765B2
Source datasetuspto-grants-2014_04
ORD IDord-ecf2977464cd442ebcfefb20ec01d0ce
Source noteuspto-grants-2014_04