HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2086205Generated: October 30, 2026
Potassium sodium tartarate → HCID 10705537, compound
https://huagongshe.com/reaction/2086205
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium sodium tartarate | HCID 9855836 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | HCID 69338221 | HCID 69338221 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10705537 | HCID 10705537 | 100% |
Reaction Steps
3-t-Butoxycarbonyl-2,2-dimethyl-(4R)-n-hexanoyloxymethyl-4-methyloxazolidine (13.7 g, 39.9 mmol) obtained in Reference example 2(a) was dissolved in dichloromethane (200 ml), and the hexane solution of 1.0M diisobutylaluminium hydride (99 ml, 99.7 mmol) was added dropwise thereto at −78° C. After, the reaction mixture was stirred for 30 minutes at −78° C., cooled down to room temperature, and 10 wt % aqueous potassium sodium tartrate solution (200 ml) was added thereto followed by stirring vigorously for 30 minutes. The reaction solution was extracted with diethyl ether, and after the ether layer was dried over anhydrous sodium sulfate, the solvent was evaporated in vacuo. The residue was purified by flash chromatography on a silica gel column (elution solvent; n-hexane:ethyl acetate=5:2) to afford the title compound (10.5 g, 100% yield) as a white crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06723745B2 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-e71cff69672a4f68be7dda4585d36096 |
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| Source note | uspto-grants-2004_04 |
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