HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759966Generated: October 24, 2026
Sodium Thiosulfate → 4-(2-Butynyloxy)-6-methanesulfonylpyrimidine
https://huagongshe.com/en/reaction/1759966
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 4-(2-Butynyloxy)-6-methylthiopyrimidine | HCID 22599877 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-(2-Butynyloxy)-6-methanesulfonylpyrimidine | HCID 22599863 | — |
Reaction Steps
To 14 ml of chloroform were added 4-(2-butynyloxy)-6-methylthiopyrimidine and 3.5 g of m-chloroperbenzoic acid (>65%), followed by stirring at 0° C. for 10 hours. The reaction mixture was then poured into a saturated aqueous sodium thiosulfate solution and extracted three times with chloroform. The chloroform layers were combined, washed with water, dried over anhydrous magnesium sulfate, and then concentrated. The residue was subjected to silica gel column chromatography to give 1.4 g of 4-(2-butynyloxy)-6-methanesulfonylpyrimidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06838463B2 |
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| Source dataset | uspto-grants-2005_01 |
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| ORD ID | ord-4fedc6ac9b4648da863d57e9b653d54c |
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| Source note | uspto-grants-2005_01 |
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