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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | (R)-2-((S)-3-benzyl-2-oxooxazolidin-4-yl)-N-methoxy-N-methylpropanamide | HCID 90414536 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Potassium Sodium Tartrate | HCID 9357 | — |
| Product | (R)-2-((S)-3-benzyl-2-oxooxazolidin-4-yl)propanal | HCID 90414373 | 105.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434719B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-c6909f475fd24092a14383f9de3b8147 |
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| Source note | uspto-grants-2016_09 |
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