HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876239Generated: October 30, 2026
Potassium bisulfate → (R)-Benzyl 4-formyl-2,2-dimethyloxazolidine-3-carboxylate
https://huagongshe.com/reaction/1876239
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | HCID 11278709 | HCID 11278709 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (R)-Benzyl 4-formyl-2,2-dimethyloxazolidine-3-carboxylate | HCID 11414364 | — |
Reaction Steps
A solution of LiALH4 (1 M, 20 mL, 20 mmol) was added dropwise to a cold (−15° C.) solution of (R)-benzyl 4-(methoxy(methyl)carbamoyl)-2,2-dimethyloxazolidine-3-carboxylate (12.2 g, 37.9 mmol) in THF (75 mL). The mixture was stirred for 30 min keeping the temperature below 0° C. A saturated solution of KHSO4 (100 mL) was added slowly to the mixture and it was warmed to room temperature. The mixture was filtered and the solvent was removed to dryness. (R)-benzyl 4-formyl-2,2-dimethyloxazolidine-3-carboxylate was obtained as a clear oil (9.161 g, 92% yield) after purification by column chromatography (SiO2, using a mixture of hexane/EtOAc). 1H NMR (CDCl3, 400 mHz, ppm); 1.7 (m, 6H), 4.15 (m, 2H), 4.4 (m, 1H), 5.15, (s, 1H), 5.2 (m, 1H), 7.3 (m, 5H), 9.6 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08309593B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-7ec26931123549f19957154e82bd27cb |
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| Source note | uspto-grants-2012_11 |
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