HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368046Generated: October 30, 2026
Lithiumtriethylborohydride → HCID 49838698, compound
https://huagongshe.com/reaction/2368046
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithiumtriethylborohydride | HCID 23664628 | — |
| Reactant | HCID 86667491 | HCID 86667491 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 49838698 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08703765B2 |
|---|
| Source dataset | uspto-grants-2014_04 |
|---|
| ORD ID | ord-ecf2977464cd442ebcfefb20ec01d0ce |
|---|
| Source note | uspto-grants-2014_04 |
|---|