HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 592268Generated: October 30, 2026
Sodium Thiosulfate → HCID 86646747, compound
https://huagongshe.com/reaction/592268
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | 2,6-Di-tert-butyl-4-methylphenol | HCID 31404 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86646748 | HCID 86646748 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 86646747 | HCID 86646747 | 423.2% |
Reaction Steps
To a solution of tert-butyl {(1R)-1-[6-(trifluoromethyl)-3-pyridinyl]ethyl}carbamate (0.626 g, 2.157 mmol) in chloroform (10.0 mL) were added 2,6-di-tert-butyl-4-methylphenol (24 mg, 0.108 mmol) and 3-chloroperbenzoic acid (0.665 g, 2.70 mmol). The reaction mixture was stirred at 50° C. for 48 h. The reaction mixture was cooled to ambient temperature. Saturated aqueous sodium thiosulfate and saturated aqueous sodium bicarbonate were added. The mixture was extracted with dichloromethane (3×). The combined organics extracts were washed with brine, dried over magnesium sulfate, filtered and concentrated. Purification by silica gel chromatography (75% hexanes/ethyl acetate 100% ethyl acetate) gave the title compound (140 mg). MS 307.0 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09238647B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-613851f9af884716be27f1c42660b03d |
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| Source note | uspto-grants-2016_01 |
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