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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192722Generated: November 1, 2026

Sodium borohydride → HCID 67083828, compound

https://huagongshe.com/reaction/2192722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-[(2R)-Tetrahydro-2-furanyl]-1-propanoneHCID 67083832—
SolventMethanolHCID 887—
ProductHCID 67083828HCID 67083828—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled (0° C.) solution of (R)-1-(tetrahydrofuran-2-yl)propan-1-one (16.16 g, 1 equiv) in MeOH was added portionwise sodium tetrahydroborate (4.77 g, 1 equiv). After stirring at 0° C. for 1 hour, the reaction was quenched with 5M HCl and allowed to stir for further for 10 minutes. The mixture was concentrated in vacuo to remove MeOH and EtOAc and water were added. The organic portion was separated and the aqueous layer extracted several times with EtOAc. The combined organic extracts were dried (MgSO4) and concentrated in vacuo to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329754B2
Source datasetuspto-grants-2012_12
ORD IDord-4a238d14a542444b9fc34eb6bf147bc3
Source noteuspto-grants-2012_12