HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22082Generated: October 26, 2026
Potassium Sodium Tartrate → (2S,3S,4S,5R)-5-(Triethylsilyloxy)-3-hydroxy-2,4-dimethyloctanal
https://huagongshe.com/reaction/22082
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Sodium Tartrate | HCID 9357 | — |
| Reactant | (2R,3S,4S,5R)-5-(Triethylsilyloxy)-2,3-epoxy-2,4-dimethyl-1-octanol | HCID 57283355 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178506586 | HCID 178506586 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2S,3S,4S,5R)-5-(Triethylsilyloxy)-3-hydroxy-2,4-dimethyloctanal | HCID 57313995 | — |
Reaction Steps
(2R,3S,4S,5R)-5-(Triethylsilyloxy)-2,3-epoxy-2,4-dimethyl-1-octanol (21.0 mg, 69.4 μmol) in 300 μl of THF at 0° C. was deprotonated with 1.05 eq of n-butyllithium. After 15 min, 0.1M samarium diiodide (764 μmol, 1.1 eq) was added and the reaction was allowed to warm to 25° C. over night. Then 1 ml of 1/2 saturated Rochelle's salt was added, stirred an additional 1 h, and poured onto 5 ml of Et2O and 1 ml of H2O. The layers were separated, extracted with ether (3×5 ml), washed with 5% NaHCO3 (2×1 ml), brine (1×1 ml), dried over MgSO4 and concentrated to give 31 crude.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05426206 |
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| Source dataset | uspto-grants-1995_06 |
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| ORD ID | ord-886f87c09f3e4a15999176d8eab283ce |
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| Source note | uspto-grants-1995_06 |
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