HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079757Generated: October 26, 2026
Water → 3-[(tert-Butyldimethylsilyloxy)methyl]-6-formyl-1,2-dithiin
https://huagongshe.com/reaction/1079757
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triacetoxyperiodinane | HCID 159087 | — |
| Reactant | 3-[(Tert-butyldimethylsilyloxy)methyl]-6-hydroxymethyl-1,2-dithiin | HCID 10062832 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-[(tert-Butyldimethylsilyloxy)methyl]-6-formyl-1,2-dithiin | HCID 11778883 | 94% |
Reaction Steps
To a solution of 3-[(tert-butyldimethylsilyloxy)methyl]-6-(hydroxymethyl)-1,2-dithiin (U.S. Ser. No. 08/212,096) (600 mg, 2.07 mmol) in THF (25 mL) at 0° C. was added quickly the Dess-Martin periodinane reagent (1.20 g, 2.83 mmol) and the mixture was stirred at 0° C. for 30 min, then at room temperature for another 30 min. Upon completion of the reaction (monitored by TLC), 12 mL of H2O was added and the mixture was extracted with ether (3×). The combined organics washings were washed with H2O, sodium hydrogen carbonate (3%-soln.), brine, dried (Na2SO4) and evaporated. Flash chromatography (eluting with hexane/EtOAc 3/1) yielded 560 mg (94%) of the title aldehyde as a dark red, almost purple, crystalline compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05580897 |
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| Source dataset | uspto-grants-1996_12 |
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| ORD ID | ord-d08a7e6211b241ebadf1660bcca7aec2 |
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| Source note | uspto-grants-1996_12 |
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