HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 76020Generated: October 29, 2026
Sodium Thiosulfate → HCID 59428142, compound
https://huagongshe.com/reaction/76020
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Triacetoxyperiodinane | HCID 159087 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 59428115 | HCID 59428115 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59428142 | HCID 59428142 | — |
Reaction Steps
To a solution of 4-tert-butyl-N-[4-chloro-2-(4-hydroxymethyl-pyrazol-1-yl)-phenyl]-benzenesulfonamide (synthesized according to general procedure LL, 31 mg, 0.074 mmol) in CH2Cl2 (3 mL) was added Dess-Martin periodinane (34 mg, 0.33 mmol) and the reaction was stirred for 3 hours at room temperature. 10% Na2S2O3 (5 mL) and saturated aqueous NaHCO3 (5 mL) were added sequentially and the mixture was stirred an additional 30 minutes. The aqueous layer was subsequently separated and extracted with EtOAc (2×25 mL). The combined organic layers were washed with saturated aqueous NaHCO3 solution (20 mL) and brine (20 mL), dried (anhydrous Na2SO4), and concentrated in vacuo to afford 4-tert-butyl-N-[4-chloro-2-(4-formyl-pyrazol-1-yl)-phenyl]-benzenesulfonamide which was used for further transformation without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835468B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-b64e566b9f0843c387d41bb6d6c07ff0 |
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| Source note | uspto-grants-2014_09 |
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