HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241291Generated: October 30, 2026
Sodium Thiosulfate → tert-Butyl [tert-butoxycarbonyl(6-formylpyridin-2-yl)amino]acetate
https://huagongshe.com/reaction/241291
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Triacetoxyperiodinane | HCID 159087 | — |
| Reactant | Tert-butyl[tert-butoxycarbonyl(6-hydroxymethylpyridin-2-yl)amino]acetate | HCID 86651768 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-Butyl [tert-butoxycarbonyl(6-formylpyridin-2-yl)amino]acetate | HCID 86651795 | 96.5% |
Reaction Steps
To a solution of Dess-martin reagent (12.9 g, 30.4 mmol) in methylene chloride (130 ml) was added dropwise a solution of tert-butyl[tert-butoxycarbonyl(6-hydroxymethylpyridin-2-yl)amino]acetate (10.0 g, 29.6 mmol) obtained in Reference Example 3-(b) in methylene chloride (50 ml) over 20 minutes under ice cooling in argon atmosphere. After completion of the dropwise addition, the mixture was stirred at room temperature for 2 hours. After completion of the reaction, a 0.1% aqueous sodium thiosulfate solution (305 ml) was added to the reaction solution, followed by extraction with methylene chloride. The separated organic layer was washed sequentially with a 0.5N aqueous sodium hydroxide solution and a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure to afford the title compound (9.61 g) substantially quantitatively as a slightly yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08648097B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-9fa938f68eb849caa5020513ed999cb1 |
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| Source note | uspto-grants-2014_02 |
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