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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57378Generated: October 29, 2026

Diisobutylaluminum hydride → (R)-2-((S)-3-benzyl-2-oxooxazolidin-4-yl)propanal

https://huagongshe.com/reaction/57378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylaluminum hydrideHCID 14487—
Reactant(R)-2-((S)-3-benzyl-2-oxooxazolidin-4-yl)-N-methoxy-N-methylpropanamideHCID 90414536—
SolventTetrahydrofuranHCID 8028—
SolventPotassium Sodium TartrateHCID 9357—
Product(R)-2-((S)-3-benzyl-2-oxooxazolidin-4-yl)propanalHCID 90414373105.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of (R)-2-((S)-3-benzyl-2-oxooxazolidin-4-yl)-N-methoxy-N-methylpropanamide from Step 6 (1.5 g, 5.13 mmol) in THF (30 mL) was added dropwise DIBAL-H (1M solution in hexane; 11.29 mL) at −78° C. The mixture was stirred for 90 min at −78° C., diluted slowly with Rochelle's salt solution (1M solution in water; ˜20 mL) and stirred vigrously for ˜15 min. The aqueous layer was separated and extracted with ethyl acetate (3×). The combined organic extracts were washed with saturated sodium bicarbonate solution and brine, filtered through a mixture of celite/silica gel. The filtrate was concentrated under reduced pressure providing crude (R)-2-((S)-3-benzyl-2-oxooxazolidin-4-yl)propanal (1.26 g) as a colorless oil, which was directly used without further purification. MS m/z 234.2 (M+H)+; Rt-0.60 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434719B2
Source datasetuspto-grants-2016_09
ORD IDord-c6909f475fd24092a14383f9de3b8147
Source noteuspto-grants-2016_09