HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061665Generated: October 27, 2026
p-Toluenesulfonic acid monohydrate → HCID 22284233, compound
https://huagongshe.com/reaction/1061665
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Methyl [(2-oxobutyl)sulfanyl]acetate | HCID 12353742 | — |
| Reactant | Methylorthoformate | HCID 53629101 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 22284233 | HCID 22284233 | — |
Reaction Steps
Methyl orthoformate (10.8 ml) and p-toluenesulfonic acid monohydrate. (catalytic amount) are added to a solution of methyl 2-(2-oxobutylthio)acetate (5.80 g, Reference compound No. 36-1) in methanol (60 ml), and the mixture is refluxed for two hours. The reaction mixture is cooled to 0° C., sodium methoxide (1.98 g) is added to the mixture, and the whole is stirred for 20 minutes. The reaction mixture is concentrated under reduced pressure, ethyl acetate is added to the resulting residue, and the whole is washed with saturated brine. The organic layer is dried over anhydrous magnesium sulfate, and the solvent is distilled away under reduced pressure to give the titled reference compound (6.85 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06960575B2 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-b8d240fab5b1451b9944a155dd46a5c8 |
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| Source note | uspto-grants-2005_11 |
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